HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38071307A= , CM000664.2:g.38071307A= | GRCh38 |
NC_000002.11:g.38298450A= , CM000664.1:g.38298450A= | GRCh37 |
NC_000002.10:g.38151954A= | NCBI36 |
NG_008386.2:g.9795T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.1047T= | ENSP00000478839.2:p.Tyr349= | |
ENST00000610745.5:c.1047T= MANE Select | ENSP00000478561.1:p.Tyr349= | |
ENST00000492443.1:n.425T= | ||
ENST00000494864.1:c.-67T= | ENSP00000479876.1:n.-67T= | |
ENST00000610745.4:c.1047T= | ENSP00000478561.1:p.Tyr349= | |
ENST00000613082.1:n.442T= | ||
ENST00000614273.1:c.1047T= | ENSP00000483678.1:p.Tyr349= | |
NM_000104.3:c.1047T= | NP_000095.2:p.Tyr349= | |
NM_000104.4:c.1047T= MANE Select | NP_000095.2:p.Tyr349= |