HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38074980A>C , CM000664.2:g.38074980A>C | GRCh38 |
NC_000002.11:g.38302123A>C , CM000664.1:g.38302123A>C | GRCh37 |
NC_000002.10:g.38155627A>C | NCBI36 |
NG_008386.2:g.6122T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.409T>G | ENSP00000478839.2:p.Tyr137Asp | |
ENST00000610745.5:c.409T>G MANE Select | ENSP00000478561.1:p.Tyr137Asp | |
ENST00000490576.1:c.409T>G | ENSP00000478839.1:p.Tyr137Asp | |
ENST00000494864.1:c.-70-3670T>G | ENSP00000479876.1:n.-70-3670T>G | |
ENST00000610745.4:c.409T>G | ENSP00000478561.1:p.Tyr137Asp | |
ENST00000613082.1:n.376-572T>G | ||
ENST00000614273.1:c.409T>G | ENSP00000483678.1:p.Tyr137Asp | |
NM_000104.3:c.409T>G | NP_000095.2:p.Tyr137Asp | |
NM_000104.4:c.409T>G MANE Select | NP_000095.2:p.Tyr137Asp |