HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55112819C= , CM000666.2:g.55112819C= | GRCh38 |
NC_000004.11:g.55978986C= , CM000666.1:g.55978986C= | GRCh37 |
NC_000004.10:g.55673743C= | NCBI36 |
NG_012004.1:g.17777G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263923.5:c.976+485G= MANE Select | ENSP00000263923.4:n.976+485G= | |
ENST00000647068.1:n.989+485G= | ||
ENST00000263923.4:c.976+485G= | ENSP00000263923.4:n.976+485G= | |
ENST00000512566.1:n.976+485G= | ||
NM_002253.2:c.976+485G= | NP_002244.1:n.976+485G= | |
NM_002253.3:c.976+485G= | NP_002244.1:n.976+485G= | |
NM_002253.4:c.976+485G= MANE Select | NP_002244.1:n.976+485G= |