Linked Data
dbSNP Id:
rs36017
gnomAD v2:
16-55718818-G-A
gnomAD v3:
16-55684906-G-A
gnomAD v4:
16-55684906-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.55684906G>A , CM000678.2:g.55684906G>A | GRCh38 |
| NC_000016.9:g.55718818G>A , CM000678.1:g.55718818G>A | GRCh37 |
| NC_000016.8:g.54276319G>A | NCBI36 |
| NG_016969.1:g.34277G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219833.13:c.645-237G>A | ENSP00000219833.8:n.645-237G>A | |
| ENST00000568943.6:c.645-237G>A MANE Select | ENSP00000457473.1:n.645-237G>A | |
| ENST00000574918.2:c.645-237G>A | ENSP00000460214.2:n.645-237G>A | |
| ENST00000682050.1:c.645-237G>A | ENSP00000508367.1:n.645-237G>A | |
| ENST00000219833.12:c.645-237G>A | ENSP00000219833.8:n.645-237G>A | |
| ENST00000379906.6:c.645-237G>A | ENSP00000369237.2:n.645-237G>A | |
| ENST00000414754.7:c.645-237G>A | ENSP00000394956.3:n.645-237G>A | |
| ENST00000561820.5:c.645-237G>A | ENSP00000454439.1:n.645-237G>A | |
| ENST00000566163.5:c.645-237G>A | ENSP00000456210.1:n.645-237G>A | |
| ENST00000567238.1:c.330-237G>A | ENSP00000457375.1:n.330-237G>A | |
| ENST00000568529.6:c.645-237G>A | ENSP00000456377.2:n.645-237G>A | |
| ENST00000568943.5:c.645-237G>A | ENSP00000457473.1:n.645-237G>A | |
| NM_001043.3:c.645-237G>A | NP_001034.1:n.645-237G>A | |
| NM_001172501.1:c.645-237G>A | NP_001165972.1:n.645-237G>A | |
| NM_001172502.1:c.330-237G>A | NP_001165973.1:n.330-237G>A | |
| NM_001172504.1:c.645-237G>A | NP_001165975.1:n.645-237G>A | |
| XM_006721263.2:c.645-237G>A | XP_006721326.1:n.645-237G>A | |
| XM_011523295.1:c.645-237G>A | XP_011521597.1:n.645-237G>A | |
| XM_011523296.1:c.645-237G>A | XP_011521598.1:n.645-237G>A | |
| XM_011523297.1:c.645-237G>A | XP_011521599.1:n.645-237G>A | |
| XM_011523298.1:c.645-237G>A | XP_011521600.1:n.645-237G>A | |
| XM_011523299.1:c.-79-237G>A | XP_011521601.1:n.-79-237G>A | |
| XM_011523300.1:c.-79-237G>A | XP_011521602.1:n.-79-237G>A | |
| XR_933403.1:n.1262-237G>A | ||
| XM_011523295.2:c.645-237G>A | XP_011521597.1:n.645-237G>A | |
| XM_011523296.2:c.645-237G>A | XP_011521598.1:n.645-237G>A | |
| XM_011523297.3:c.645-237G>A | XP_011521599.1:n.645-237G>A | |
| XM_011523298.2:c.645-237G>A | XP_011521600.1:n.645-237G>A | |
| XM_011523299.2:c.-79-237G>A | XP_011521601.1:n.-79-237G>A | |
| XM_011523300.2:c.-79-237G>A | XP_011521602.1:n.-79-237G>A | |
| XR_933403.3:n.938-237G>A | ||
| NM_001172501.2:c.645-237G>A | NP_001165972.1:n.645-237G>A | |
| NM_001172501.3:c.645-237G>A MANE Select | NP_001165972.1:n.645-237G>A |