HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640434T>C , CM000673.2:g.640434T>C | GRCh38 |
NC_000011.9:g.640434T>C , CM000673.1:g.640434T>C | GRCh37 |
NC_000011.8:g.630434T>C | NCBI36 |
NG_021241.1:g.8130T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000176183.6:c.1091T>C MANE Select | ENSP00000176183.5:p.Val364Ala | |
ENST00000176183.5:c.1091T>C | ENSP00000176183.5:p.Val364Ala | |
NM_000797.3:c.1091T>C | NP_000788.2:p.Val364Ala | |
NM_000797.4:c.1091T>C MANE Select | NP_000788.2:p.Val364Ala |