Linked Data
dbSNP Id:
rs2072909998
gnomAD v3:
15-74180235-G-A
gnomAD v4:
15-74180235-G-A
MyVariant Identifiers:
chr15:g.74472576G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74180235G>A , CM000677.2:g.74180235G>A | GRCh38 |
| NC_000015.9:g.74472576G>A , CM000677.1:g.74472576G>A | GRCh37 |
| NC_000015.8:g.72259629G>A | NCBI36 |
| NG_009207.1:g.33796C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395105.9:c.1849C>T MANE Select | ENSP00000378537.4:p.Leu617= | |
| ENST00000323940.9:c.1849C>T | ENSP00000326085.5:p.Leu617= | |
| ENST00000395105.8:c.1849C>T | ENSP00000378537.4:p.Leu617= | |
| ENST00000416286.7:c.1825C>T | ENSP00000400403.3:p.Leu609= | |
| ENST00000423167.6:c.1822C>T | ENSP00000413012.2:p.Leu608= | |
| ENST00000449139.6:c.1849C>T | ENSP00000410221.2:p.Leu617= | |
| ENST00000535552.5:c.1960C>T | ENSP00000440238.1:p.Leu654= | |
| ENST00000545137.5:n.1558C>T | ||
| ENST00000563965.5:c.1966C>T | ENSP00000456609.1:p.Leu656= | |
| ENST00000572785.1:c.704C>T | ||
| ENST00000574278.5:c.1894C>T | ENSP00000458827.1:p.Leu632= | |
| ENST00000574439.5:n.2121C>T | ||
| ENST00000616000.4:c.1849C>T | ENSP00000479112.1:p.Leu617= | |
| NM_001142617.1:c.1849C>T | NP_001136089.1:p.Leu617= | |
| NM_001142618.1:c.1849C>T | NP_001136090.1:p.Leu617= | |
| NM_001142619.1:c.1822C>T | NP_001136091.1:p.Leu608= | |
| NM_001199040.1:c.1960C>T | NP_001185969.1:p.Leu654= | |
| NM_001199041.1:c.1894C>T | NP_001185970.1:p.Leu632= | |
| NM_001199042.1:c.1966C>T | NP_001185971.1:p.Leu656= | |
| NM_022369.3:c.1849C>T | NP_071764.3:p.Leu617= | |
| XM_011521883.1:c.1849C>T | XP_011520185.1:p.Leu617= | |
| XM_011521884.1:c.1660C>T | XP_011520186.1:p.Leu554= | |
| XM_017022478.1:c.1897C>T | XP_016877967.1:p.Leu633= | |
| XM_017022479.1:c.1849C>T | XP_016877968.1:p.Leu617= | |
| XM_017022480.1:c.1660C>T | XP_016877969.1:p.Leu554= | |
| NM_022369.4:c.1849C>T MANE Select | NP_071764.3:p.Leu617= | |
| NM_001142617.2:c.1849C>T | NP_001136089.1:p.Leu617= | |
| NM_001142619.2:c.1822C>T | NP_001136091.1:p.Leu608= | |
| NM_001199042.2:c.1966C>T | NP_001185971.1:p.Leu656= | |
| NM_001142618.2:c.1849C>T | NP_001136090.1:p.Leu617= | |
| NM_001199040.2:c.1960C>T | NP_001185969.1:p.Leu654= | |
| NM_001199041.2:c.1894C>T | NP_001185970.1:p.Leu632= |