HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128261667T>G , CM000667.2:g.128261667T>G | GRCh38 |
NC_000005.9:g.127597359T>G , CM000667.1:g.127597359T>G | GRCh37 |
NC_000005.8:g.127625258T>G | NCBI36 |
NG_008750.1:g.281377A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.8364+69A>C MANE Select | ENSP00000262464.4:n.8364+69A>C | |
ENST00000262464.8:c.8364+69A>C | ENSP00000262464.4:n.8364+69A>C | |
ENST00000508053.5:c.8364+69A>C | ENSP00000424571.1:n.8364+69A>C | |
ENST00000619499.4:c.8361+69A>C | ENSP00000482132.1:n.8361+69A>C | |
NM_001999.3:c.8364+69A>C | NP_001990.2:n.8364+69A>C | |
XM_017009228.2:c.8211+69A>C | XP_016864717.1:n.8211+69A>C | |
NM_001999.4:c.8364+69A>C MANE Select | NP_001990.2:n.8364+69A>C |