HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55091441T= , CM000666.2:g.55091441T= | GRCh38 |
NC_000004.11:g.55957608T= , CM000666.1:g.55957608T= | GRCh37 |
NC_000004.10:g.55652365T= | NCBI36 |
NG_012004.1:g.39155A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.3069+1176A= MANE Select | ENSP00000263923.4:n.3069+1176A= | |
ENST00000647068.1:n.3082+1176A= | ||
ENST00000263923.4:c.3069+1176A= | ENSP00000263923.4:n.3069+1176A= | |
NM_002253.2:c.3069+1176A= | NP_002244.1:n.3069+1176A= | |
NM_002253.3:c.3069+1176A= | NP_002244.1:n.3069+1176A= | |
NM_002253.4:c.3069+1176A= MANE Select | NP_002244.1:n.3069+1176A= |