HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38070765T= , CM000664.2:g.38070765T= | GRCh38 |
NC_000002.11:g.38297908T= , CM000664.1:g.38297908T= | GRCh37 |
NC_000002.10:g.38151412T= | NCBI36 |
NG_008386.2:g.10337A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000490576.2:c.1589A= | ENSP00000478839.2:p.Asp530= | |
ENST00000610745.5:c.1589A= MANE Select | ENSP00000478561.1:p.Asp530= | |
ENST00000494864.1:c.476A= | ENSP00000479876.1:p.Asp159= | |
ENST00000610745.4:c.1589A= | ENSP00000478561.1:p.Asp530= | |
ENST00000614273.1:c.1589A= | ENSP00000483678.1:p.Asp530= | |
NM_000104.3:c.1589A= | NP_000095.2:p.Asp530= | |
NM_000104.4:c.1589A= MANE Select | NP_000095.2:p.Asp530= |