Linked Data
ClinVar Variation Id:
353985
dbSNP Id:
rs538879121
gnomAD v2:
5-58270662-G-A
gnomAD v3:
5-58974835-G-A
gnomAD v4:
5-58974835-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.58974835G>A , CM000667.2:g.58974835G>A | GRCh38 |
| NC_000005.9:g.58270662G>A , CM000667.1:g.58270662G>A | GRCh37 |
| NC_000005.8:g.58306419G>A | NCBI36 |
| NG_027957.1:g.1518264C>T | |
| NG_027957.2:g.1554495C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507116.6:c.2067C>T | ENSP00000424852.1:p.Gly689= | |
| ENST00000340635.11:c.2259C>T MANE Select | ENSP00000345502.6:p.Gly753= | |
| ENST00000636120.1:c.1929C>T | ENSP00000490821.1:p.Gly643= | |
| ENST00000317118.12:c.1386C>T | ENSP00000321739.8:p.Gly462= | |
| ENST00000340635.10:c.2259C>T | ENSP00000345502.6:p.Gly753= | |
| ENST00000358923.10:c.1353C>T | ENSP00000351800.6:p.Gly451= | |
| ENST00000360047.9:c.1851C>T | ENSP00000353152.5:p.Gly617= | |
| ENST00000405755.6:c.1893C>T | ENSP00000384806.2:p.Gly631= | |
| ENST00000502484.6:c.2076C>T | ENSP00000423094.2:p.Gly692= | |
| ENST00000503258.5:c.1869C>T | ENSP00000425605.1:p.Gly623= | |
| ENST00000507116.5:c.2067C>T | ENSP00000424852.1:p.Gly689= | |
| ENST00000515011.5:n.1995C>T | ||
| ENST00000546160.5:c.1866C>T | ENSP00000442734.2:p.Gly622= | |
| NM_001104631.1:c.2259C>T | NP_001098101.1:p.Gly753= | |
| NM_001165899.1:c.2076C>T | NP_001159371.1:p.Gly692= | |
| NM_001197218.1:c.2067C>T | NP_001184147.1:p.Gly689= | |
| NM_001197219.1:c.1893C>T | NP_001184148.1:p.Gly631= | |
| NM_001197220.1:c.1869C>T | NP_001184149.1:p.Gly623= | |
| NM_001197221.1:c.1353C>T | NP_001184150.1:p.Gly451= | |
| NM_001197222.1:c.1587C>T | NP_001184151.1:p.Gly529= | |
| NM_001197223.1:c.1386C>T | NP_001184152.1:p.Gly462= | |
| NM_006203.4:c.1851C>T | NP_006194.2:p.Gly617= | |
| XM_005248537.2:c.1929C>T | XP_005248594.1:p.Gly643= | |
| XM_005248538.3:c.1851C>T | XP_005248595.1:p.Gly617= | |
| XM_011543469.1:c.2223C>T | XP_011541771.1:p.Gly741= | |
| XM_011543470.1:c.2223C>T | XP_011541772.1:p.Gly741= | |
| XM_011543471.1:c.2076C>T | XP_011541773.1:p.Gly692= | |
| XM_011543472.1:c.2076C>T | XP_011541774.1:p.Gly692= | |
| XM_011543473.1:c.2076C>T | XP_011541775.1:p.Gly692= | |
| XM_011543474.1:c.2046C>T | XP_011541776.1:p.Gly682= | |
| XM_011543475.1:c.1893C>T | XP_011541777.1:p.Gly631= | |
| XM_011543476.1:c.1839C>T | XP_011541778.1:p.Gly613= | |
| XM_011543477.1:c.1818C>T | XP_011541779.1:p.Gly606= | |
| XM_011543478.1:c.1755C>T | XP_011541780.1:p.Gly585= | |
| XM_011543479.1:c.1755C>T | XP_011541781.1:p.Gly585= | |
| NM_001349241.1:c.2046C>T | NP_001336170.1:p.Gly682= | |
| NM_001349242.1:c.1929C>T | NP_001336171.1:p.Gly643= | |
| NM_001349243.1:c.1491C>T | NP_001336172.1:p.Gly497= | |
| NM_001364599.1:c.2076C>T | NP_001351528.1:p.Gly692= | |
| NM_001364603.1:c.1353C>T | NP_001351532.1:p.Gly451= | |
| NM_001364604.1:c.1491C>T | NP_001351533.1:p.Gly497= | |
| XM_011543470.2:c.2223C>T | XP_011541772.1:p.Gly741= | |
| XM_011543471.2:c.2076C>T | XP_011541773.1:p.Gly692= | |
| XM_017009565.1:c.2223C>T | XP_016865054.1:p.Gly741= | |
| XM_017009566.1:c.2076C>T | XP_016865055.1:p.Gly692= | |
| XM_017009567.1:c.2061C>T | XP_016865056.1:p.Gly687= | |
| XM_024446110.1:c.2223C>T | XP_024301878.1:p.Gly741= | |
| XM_024446112.1:c.2076C>T | XP_024301880.1:p.Gly692= | |
| NM_001104631.2:c.2259C>T MANE Select | NP_001098101.1:p.Gly753= | |
| NM_001165899.2:c.2076C>T | NP_001159371.1:p.Gly692= | |
| NM_001197218.2:c.2067C>T | NP_001184147.1:p.Gly689= | |
| NM_001197219.2:c.1893C>T | NP_001184148.1:p.Gly631= | |
| NM_001197220.2:c.1869C>T | NP_001184149.1:p.Gly623= | |
| NM_001197221.2:c.1353C>T | NP_001184150.1:p.Gly451= | |
| NM_001197222.2:c.1587C>T | NP_001184151.1:p.Gly529= | |
| NM_001197223.2:c.1386C>T | NP_001184152.1:p.Gly462= | |
| NM_001349241.2:c.2046C>T | NP_001336170.1:p.Gly682= | |
| NM_001349243.2:c.1491C>T | NP_001336172.1:p.Gly497= | |
| NM_001349242.2:c.1929C>T | NP_001336171.1:p.Gly643= | |
| NM_006203.5:c.1851C>T | NP_006194.2:p.Gly617= |