HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81535499A>T , CM000665.2:g.81535499A>T | GRCh38 |
NC_000003.11:g.81584650A>T , CM000665.1:g.81584650A>T | GRCh37 |
NC_000003.10:g.81667340A>T | NCBI36 |
NG_011810.1:g.231302T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.1804-174T>A MANE Select | ENSP00000410833.2:n.1804-174T>A | |
ENST00000429644.6:c.1804-174T>A | ENSP00000410833.2:n.1804-174T>A | |
ENST00000484687.1:n.205-174T>A | ||
ENST00000489715.1:c.1681-174T>A | ENSP00000419638.1:n.1681-174T>A | |
NM_000158.3:c.1804-174T>A | NP_000149.3:n.1804-174T>A | |
NM_000158.4:c.1804-174T>A MANE Select | NP_000149.4:n.1804-174T>A |