HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129529333T>A , CM000665.2:g.129529333T>A | GRCh38 |
NC_000003.11:g.129248176T>A , CM000665.1:g.129248176T>A | GRCh37 |
NC_000003.10:g.130730866T>A | NCBI36 |
NG_009115.1:g.5695T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.361+239T>A MANE Select | ENSP00000296271.3:n.361+239T>A | |
ENST00000296271.3:c.361+239T>A | ENSP00000296271.3:n.361+239T>A | |
NM_000539.3:c.361+239T>A MANE Select | NP_000530.1:n.361+239T>A |