HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107325G>T , CM000674.2:g.91107325G>T | GRCh38 |
NC_000012.11:g.91501102G>T , CM000674.1:g.91501102G>T | GRCh37 |
NC_000012.10:g.90025233G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+793C>A MANE Select | ENSP00000266718.4:n.862+793C>A | |
ENST00000266718.4:c.862+793C>A | ENSP00000266718.4:n.862+793C>A | |
ENST00000546642.1:n.612+793C>A | ||
ENST00000548071.1:n.255+793C>A | ||
NM_002345.3:c.862+793C>A | NP_002336.1:n.862+793C>A | |
NM_002345.4:c.862+793C>A MANE Select | NP_002336.1:n.862+793C>A |