Linked Data
dbSNP Id:
rs763921537
ExAC:
17:1554578 G / A
gnomAD v2:
17-1554578-G-A
gnomAD v4:
17-1651284-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.1651284G>A , CM000679.2:g.1651284G>A | GRCh38 |
| NC_000017.10:g.1554578G>A , CM000679.1:g.1554578G>A | GRCh37 |
| NC_000017.9:g.1501328G>A | NCBI36 |
| NG_009118.1:g.38599C>T | |
| NG_033061.1:g.3815C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000573725.2:c.6497C>T | ENSP00000460849.2:p.Thr2166Met | |
| ENST00000703537.1:c.2425C>T | ||
| ENST00000703538.1:c.*6400C>T | ENSP00000515361.1:n.*6400C>T | |
| ENST00000703539.1:n.2991C>T | ||
| ENST00000703540.1:c.6530C>T | ENSP00000515362.1:p.Thr2177Met | |
| ENST00000703541.1:c.6542C>T | ENSP00000515363.1:p.Thr2181Met | |
| ENST00000304992.11:c.6677C>T MANE Select | ENSP00000304350.6:p.Thr2226Met | |
| ENST00000304992.10:c.6677C>T | ENSP00000304350.6:p.Thr2226Met | |
| ENST00000572621.5:c.6677C>T | ENSP00000460348.1:p.Thr2226Met | |
| ENST00000572723.1:n.666C>T | ||
| NM_006445.3:c.6677C>T | NP_006436.3:p.Thr2226Met | |
| XM_024450537.1:c.6677C>T | XP_024306305.1:p.Thr2226Met | |
| NM_006445.4:c.6677C>T MANE Select | NP_006436.3:p.Thr2226Met |