HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81535486G>A , CM000665.2:g.81535486G>A | GRCh38 |
NC_000003.11:g.81584637G>A , CM000665.1:g.81584637G>A | GRCh37 |
NC_000003.10:g.81667327G>A | NCBI36 |
NG_011810.1:g.231315C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.1804-161C>T MANE Select | ENSP00000410833.2:n.1804-161C>T | |
ENST00000429644.6:c.1804-161C>T | ENSP00000410833.2:n.1804-161C>T | |
ENST00000484687.1:n.205-161C>T | ||
ENST00000489715.1:c.1681-161C>T | ENSP00000419638.1:n.1681-161C>T | |
NM_000158.3:c.1804-161C>T | NP_000149.3:n.1804-161C>T | |
NM_000158.4:c.1804-161C>T MANE Select | NP_000149.4:n.1804-161C>T |