HGVS | Genome Assembly |
---|---|
NC_000020.11:g.32859026G>T , CM000682.2:g.32859026G>T | GRCh38 |
NC_000020.10:g.31446832G>T , CM000682.1:g.31446832G>T | GRCh37 |
NC_000020.9:g.30910493G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400522.9:c.-11+20G>T MANE Select | ENSP00000383366.5:n.-11+20G>T | |
ENST00000400522.8:c.-11+20G>T | ENSP00000383366.5:n.-11+20G>T | |
NM_001143967.1:c.-11+20G>T | NP_001137439.1:n.-11+20G>T | |
XM_024451882.1:c.-11+20G>T | XP_024307650.1:n.-11+20G>T | |
XM_024451883.1:c.-11+20G>T | XP_024307651.1:n.-11+20G>T | |
XM_024451885.1:c.-11+20G>T | XP_024307653.1:n.-11+20G>T | |
NM_001143967.2:c.-11+20G>T MANE Select | NP_001137439.1:n.-11+20G>T |