HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55112836T= , CM000666.2:g.55112836T= | GRCh38 |
NC_000004.11:g.55979003T= , CM000666.1:g.55979003T= | GRCh37 |
NC_000004.10:g.55673760T= | NCBI36 |
NG_012004.1:g.17760A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263923.5:c.976+468A= MANE Select | ENSP00000263923.4:n.976+468A= | |
ENST00000647068.1:n.989+468A= | ||
ENST00000263923.4:c.976+468A= | ENSP00000263923.4:n.976+468A= | |
ENST00000512566.1:n.976+468A= | ||
NM_002253.2:c.976+468A= | NP_002244.1:n.976+468A= | |
NM_002253.3:c.976+468A= | NP_002244.1:n.976+468A= | |
NM_002253.4:c.976+468A= MANE Select | NP_002244.1:n.976+468A= |