HGVS | Genome Assembly |
---|---|
NC_000011.10:g.639981T>A , CM000673.2:g.639981T>A | GRCh38 |
NC_000011.9:g.639981T>A , CM000673.1:g.639981T>A | GRCh37 |
NC_000011.8:g.629981T>A | NCBI36 |
NG_021241.1:g.7677T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.732T>A MANE Select | ENSP00000176183.5:p.Pro244= | |
ENST00000176183.5:c.732T>A | ENSP00000176183.5:p.Pro244= | |
NM_000797.3:c.732T>A | NP_000788.2:p.Pro244= | |
NM_000797.4:c.732T>A MANE Select | NP_000788.2:p.Pro244= |