HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816709C>A , CM000681.2:g.4816709C>A | GRCh38 |
NC_000019.9:g.4816721C>A , CM000681.1:g.4816721C>A | GRCh37 |
NC_000019.8:g.4767721C>A | NCBI36 |
NG_031998.1:g.20034G>T , LRG_358:g.20034G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.1669G>T MANE Select | ENSP00000248244.4:p.Asp557Tyr | |
ENST00000248244.5:c.1669G>T | ENSP00000248244.4:p.Asp557Tyr | |
ENST00000621756.1:c.1252G>T | ENSP00000479467.1:p.Asp418Tyr | |
NM_182919.3:c.1669G>T , LRG_358t1:c.1669G>T | NP_891549.1:p.Asp557Tyr | |
NM_001385678.1:c.1627G>T | NP_001372607.1:p.Asp543Tyr | |
NM_001385679.1:c.1534G>T | NP_001372608.1:p.Asp512Tyr | |
NM_001385680.1:c.1027G>T | NP_001372609.1:p.Asp343Tyr | |
NM_182919.4:c.1669G>T MANE Select | NP_891549.1:p.Asp557Tyr |