HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128344390C>T , CM000667.2:g.128344390C>T | GRCh38 |
NC_000005.9:g.127680082C>T , CM000667.1:g.127680082C>T | GRCh37 |
NC_000005.8:g.127707981C>T | NCBI36 |
NG_008750.1:g.198654G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262464.9:c.3338G>A MANE Select | ENSP00000262464.4:p.Cys1113Tyr | |
ENST00000262464.8:c.3338G>A | ENSP00000262464.4:p.Cys1113Tyr | |
ENST00000508053.5:c.3338G>A | ENSP00000424571.1:p.Cys1113Tyr | |
ENST00000508989.5:c.3239G>A | ENSP00000425596.1:p.Cys1080Tyr | |
ENST00000619499.4:c.3335G>A | ENSP00000482132.1:p.Cys1112Tyr | |
NM_001999.3:c.3338G>A | NP_001990.2:p.Cys1113Tyr | |
XM_017009228.2:c.3185G>A | XP_016864717.1:p.Cys1062Tyr | |
NM_001999.4:c.3338G>A MANE Select | NP_001990.2:p.Cys1113Tyr |