HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646313A>G , CM000665.2:g.81646313A>G | GRCh38 |
NC_000003.11:g.81695464A>G , CM000665.1:g.81695464A>G | GRCh37 |
NC_000003.10:g.81778154A>G | NCBI36 |
NG_011810.1:g.120488T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.782+79T>C MANE Select | ENSP00000410833.2:n.782+79T>C | |
ENST00000429644.6:c.782+79T>C | ENSP00000410833.2:n.782+79T>C | |
ENST00000489715.1:c.659+79T>C | ENSP00000419638.1:n.659+79T>C | |
ENST00000498468.1:n.332+79T>C | ||
NM_000158.3:c.782+79T>C | NP_000149.3:n.782+79T>C | |
NM_000158.4:c.782+79T>C MANE Select | NP_000149.4:n.782+79T>C |