HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816642G>T , CM000681.2:g.4816642G>T | GRCh38 |
NC_000019.9:g.4816654G>T , CM000681.1:g.4816654G>T | GRCh37 |
NC_000019.8:g.4767654G>T | NCBI36 |
NG_031998.1:g.20101C>A , LRG_358:g.20101C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.1736C>A MANE Select | ENSP00000248244.4:p.Ser579Tyr | |
ENST00000248244.5:c.1736C>A | ENSP00000248244.4:p.Ser579Tyr | |
ENST00000621756.1:c.1319C>A | ENSP00000479467.1:p.Ser440Tyr | |
NM_182919.3:c.1736C>A , LRG_358t1:c.1736C>A | NP_891549.1:p.Ser579Tyr | |
NM_001385678.1:c.1694C>A | NP_001372607.1:p.Ser565Tyr | |
NM_001385679.1:c.1601C>A | NP_001372608.1:p.Ser534Tyr | |
NM_001385680.1:c.1094C>A | NP_001372609.1:p.Ser365Tyr | |
NM_182919.4:c.1736C>A MANE Select | NP_891549.1:p.Ser579Tyr |