HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1414656A>T , CM000667.2:g.1414656A>T | GRCh38 |
NC_000005.9:g.1414771A>T , CM000667.1:g.1414771A>T | GRCh37 |
NC_000005.8:g.1467771A>T | NCBI36 |
NG_015885.1:g.35773T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1156+35T>A MANE Select | ENSP00000270349.9:n.1156+35T>A | |
ENST00000270349.11:c.1156+35T>A | ENSP00000270349.9:n.1156+35T>A | |
NM_001044.4:c.1156+35T>A | NP_001035.1:n.1156+35T>A | |
NM_001044.5:c.1156+35T>A MANE Select | NP_001035.1:n.1156+35T>A |