HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128304961G>C , CM000667.2:g.128304961G>C | GRCh38 |
NC_000005.9:g.127640653G>C , CM000667.1:g.127640653G>C | GRCh37 |
NC_000005.8:g.127668552G>C | NCBI36 |
NG_008750.1:g.238083C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703783.1:n.2580C>G | ||
ENST00000703785.1:n.2499C>G | ||
ENST00000262464.9:c.5796C>G MANE Select | ENSP00000262464.4:p.Cys1932Trp | |
ENST00000262464.8:c.5796C>G | ENSP00000262464.4:p.Cys1932Trp | |
ENST00000508053.5:c.5796C>G | ENSP00000424571.1:p.Cys1932Trp | |
ENST00000619499.4:c.5793C>G | ENSP00000482132.1:p.Cys1931Trp | |
NM_001999.3:c.5796C>G | NP_001990.2:p.Cys1932Trp | |
XM_017009228.2:c.5643C>G | XP_016864717.1:p.Cys1881Trp | |
NM_001999.4:c.5796C>G MANE Select | NP_001990.2:p.Cys1932Trp |