HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128344391A>T , CM000667.2:g.128344391A>T | GRCh38 |
NC_000005.9:g.127680083A>T , CM000667.1:g.127680083A>T | GRCh37 |
NC_000005.8:g.127707982A>T | NCBI36 |
NG_008750.1:g.198653T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262464.9:c.3337T>A MANE Select | ENSP00000262464.4:p.Cys1113Ser | |
ENST00000262464.8:c.3337T>A | ENSP00000262464.4:p.Cys1113Ser | |
ENST00000508053.5:c.3337T>A | ENSP00000424571.1:p.Cys1113Ser | |
ENST00000508989.5:c.3238T>A | ENSP00000425596.1:p.Cys1080Ser | |
ENST00000619499.4:c.3334T>A | ENSP00000482132.1:p.Cys1112Ser | |
NM_001999.3:c.3337T>A | NP_001990.2:p.Cys1113Ser | |
XM_017009228.2:c.3184T>A | XP_016864717.1:p.Cys1062Ser | |
NM_001999.4:c.3337T>A MANE Select | NP_001990.2:p.Cys1113Ser |