Linked Data
ClinVar Variation Id:
418274
dbSNP Id:
rs575162600
ExAC:
9:138662242 G / A
gnomAD v2:
9-138662242-G-A
gnomAD v3:
9-135770396-G-A
gnomAD v4:
9-135770396-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135770396G>A , CM000671.2:g.135770396G>A | GRCh38 |
| NC_000009.11:g.138662242G>A , CM000671.1:g.138662242G>A | GRCh37 |
| NC_000009.10:g.137802063G>A | NCBI36 |
| NG_033070.1:g.73212G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.1718G>A MANE Select | ENSP00000360822.2:p.Arg573His | |
| ENST00000674572.1:c.1559G>A | ENSP00000501742.1:p.Arg520His | |
| ENST00000675090.1:c.1466G>A | ENSP00000501833.1:p.Arg489His | |
| ENST00000675399.1:c.1466G>A | ENSP00000501932.1:p.Arg489His | |
| ENST00000676421.1:c.1475G>A | ENSP00000502322.1:p.Arg492His | |
| ENST00000263604.5:c.1619G>A | ENSP00000263604.4:p.Arg540His | |
| ENST00000371757.6:c.1718G>A | ENSP00000360822.2:p.Arg573His | |
| ENST00000460750.5:c.*1328G>A | ENSP00000418777.1:n.*1328G>A | |
| ENST00000486577.6:c.1601G>A | ENSP00000417578.3:p.Arg534His | |
| ENST00000487664.5:c.1718G>A | ENSP00000417851.2:p.Arg573His | |
| ENST00000488444.6:c.1661G>A | ENSP00000419007.3:p.Arg554His | |
| ENST00000490355.6:c.1661G>A | ENSP00000418003.3:p.Arg554His | |
| ENST00000490363.3:n.1537G>A | ||
| ENST00000491806.6:c.1661G>A | ENSP00000419086.3:p.Arg554His | |
| ENST00000628528.2:c.1583G>A | ENSP00000486374.1:p.Arg528His | |
| ENST00000630792.2:c.1559G>A | ENSP00000486486.1:p.Arg520His | |
| ENST00000631073.2:c.1661G>A | ENSP00000486130.1:p.Arg554His | |
| NM_001272003.1:c.1583G>A | NP_001258932.1:p.Arg528His | |
| NM_020822.2:c.1718G>A | NP_065873.2:p.Arg573His | |
| XM_011518877.1:c.1853G>A | XP_011517179.1:p.Arg618His | |
| XM_011518878.1:c.1862G>A | XP_011517180.1:p.Arg621His | |
| XM_011518879.1:c.1853G>A | XP_011517181.1:p.Arg618His | |
| XM_011518880.1:c.1619G>A | XP_011517182.1:p.Arg540His | |
| XM_011518881.1:c.1208G>A | XP_011517183.1:p.Arg403His | |
| XM_011518877.3:c.1853G>A | XP_011517179.1:p.Arg618His | |
| XM_011518878.3:c.1862G>A | XP_011517180.1:p.Arg621His | |
| XM_011518879.3:c.1853G>A | XP_011517181.1:p.Arg618His | |
| XM_011518881.3:c.1208G>A | XP_011517183.1:p.Arg403His | |
| XM_017014931.1:c.1652G>A | XP_016870420.1:p.Arg551His | |
| XM_017014932.1:c.1475G>A | XP_016870421.1:p.Arg492His | |
| XM_017014933.1:c.1208G>A | XP_016870422.1:p.Arg403His | |
| XM_024447617.1:c.1208G>A | XP_024303385.1:p.Arg403His | |
| XM_024447618.1:c.1208G>A | XP_024303386.1:p.Arg403His | |
| NM_020822.3:c.1718G>A MANE Select | NP_065873.2:p.Arg573His | |
| NM_001272003.2:c.1583G>A | NP_001258932.1:p.Arg528His |