HGVS | Genome Assembly |
---|---|
NC_000014.9:g.49621761G= , CM000676.2:g.49621761G= | GRCh38 |
NC_000014.8:g.50088479G= , CM000676.1:g.50088479G= | GRCh37 |
NC_000014.7:g.49158229G= | NCBI36 |
NG_008920.1:g.5991G= | |
NG_033054.1:g.3871C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305386.4:c.493G= MANE Select | ENSP00000307423.2:p.Ala165= | |
ENST00000305386.3:c.493G= | ENSP00000307423.2:p.Ala165= | |
NM_002408.3:c.493G= | NP_002399.1:p.Ala165= | |
NM_002408.4:c.493G= MANE Select | NP_002399.1:p.Ala165= |