HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38071303C>A , CM000664.2:g.38071303C>A | GRCh38 |
NC_000002.11:g.38298446C>A , CM000664.1:g.38298446C>A | GRCh37 |
NC_000002.10:g.38151950C>A | NCBI36 |
NG_008386.2:g.9799G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.1051G>T | ENSP00000478839.2:p.Asp351Tyr | |
ENST00000610745.5:c.1051G>T MANE Select | ENSP00000478561.1:p.Asp351Tyr | |
ENST00000492443.1:n.429G>T | ||
ENST00000494864.1:c.-63G>T | ENSP00000479876.1:n.-63G>T | |
ENST00000610745.4:c.1051G>T | ENSP00000478561.1:p.Asp351Tyr | |
ENST00000613082.1:n.446G>T | ||
ENST00000614273.1:c.1051G>T | ENSP00000483678.1:p.Asp351Tyr | |
NM_000104.3:c.1051G>T | NP_000095.2:p.Asp351Tyr | |
NM_000104.4:c.1051G>T MANE Select | NP_000095.2:p.Asp351Tyr |