HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119414280C= , CM000665.2:g.119414280C= | GRCh38 |
NC_000003.11:g.119133127C= , CM000665.1:g.119133127C= | GRCh37 |
NC_000003.10:g.120615817C= | NCBI36 |
NG_007665.2:g.124908C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2351C= MANE Select | ENSP00000264245.4:p.Ala784= | |
ENST00000264245.8:c.2351C= | ENSP00000264245.4:p.Ala784= | |
NM_020754.3:c.2351C= | NP_065805.2:p.Ala784= | |
XM_005247671.3:c.2258C= | XP_005247728.1:p.Ala753= | |
XM_006713714.2:c.2291C= | XP_006713777.1:p.Ala764= | |
XM_006713714.3:c.2291C= | XP_006713777.1:p.Ala764= | |
XM_017006955.1:c.1859C= | XP_016862444.1:p.Ala620= | |
NM_020754.4:c.2351C= MANE Select | NP_065805.2:p.Ala784= |