HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107051T>G , CM000674.2:g.91107051T>G | GRCh38 |
NC_000012.11:g.91500828T>G , CM000674.1:g.91500828T>G | GRCh37 |
NC_000012.10:g.90024959T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+1067A>C MANE Select | ENSP00000266718.4:n.862+1067A>C | |
ENST00000266718.4:c.862+1067A>C | ENSP00000266718.4:n.862+1067A>C | |
ENST00000546642.1:n.612+1067A>C | ||
ENST00000548071.1:n.255+1067A>C | ||
NM_002345.3:c.862+1067A>C | NP_002336.1:n.862+1067A>C | |
NM_002345.4:c.862+1067A>C MANE Select | NP_002336.1:n.862+1067A>C |