HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413877G>T , CM000665.2:g.119413877G>T | GRCh38 |
NC_000003.11:g.119132724G>T , CM000665.1:g.119132724G>T | GRCh37 |
NC_000003.10:g.120615414G>T | NCBI36 |
NG_007665.2:g.124505G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264245.9:c.1948G>T MANE Select | ENSP00000264245.4:p.Ala650Ser | |
ENST00000264245.8:c.1948G>T | ENSP00000264245.4:p.Ala650Ser | |
NM_020754.3:c.1948G>T | NP_065805.2:p.Ala650Ser | |
XM_005247671.3:c.1855G>T | XP_005247728.1:p.Ala619Ser | |
XM_006713714.2:c.1888G>T | XP_006713777.1:p.Ala630Ser | |
XM_006713714.3:c.1888G>T | XP_006713777.1:p.Ala630Ser | |
XM_017006955.1:c.1456G>T | XP_016862444.1:p.Ala486Ser | |
NM_020754.4:c.1948G>T MANE Select | NP_065805.2:p.Ala650Ser |