HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55124998C>T , CM000666.2:g.55124998C>T | GRCh38 |
NC_000004.11:g.55991165C>T , CM000666.1:g.55991165C>T | GRCh37 |
NC_000004.10:g.55685922C>T | NCBI36 |
NG_012004.1:g.5598G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.67+229G>A MANE Select | ENSP00000263923.4:n.67+229G>A | |
ENST00000263923.4:c.67+229G>A | ENSP00000263923.4:n.67+229G>A | |
ENST00000512566.1:n.67+229G>A | ||
NM_002253.2:c.67+229G>A | NP_002244.1:n.67+229G>A | |
NM_002253.3:c.67+229G>A | NP_002244.1:n.67+229G>A | |
NM_002253.4:c.67+229G>A MANE Select | NP_002244.1:n.67+229G>A |