HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118947863T>A , CM000670.2:g.118947863T>A | GRCh38 |
NC_000008.10:g.119960102T>A , CM000670.1:g.119960102T>A | GRCh37 |
NC_000008.9:g.120029283T>A | NCBI36 |
NG_012202.1:g.9282A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297350.9:c.30+3929A>T MANE Select | ENSP00000297350.4:n.30+3929A>T | |
ENST00000297350.8:c.30+3929A>T | ENSP00000297350.4:n.30+3929A>T | |
ENST00000517352.1:c.30+3929A>T | ENSP00000427924.1:n.30+3929A>T | |
NM_002546.3:c.30+3929A>T | NP_002537.3:n.30+3929A>T | |
NM_002546.4:c.30+3929A>T MANE Select | NP_002537.3:n.30+3929A>T |