HGVS | Genome Assembly |
---|---|
NC_000011.10:g.44265126C>T , CM000673.2:g.44265126C>T | GRCh38 |
NC_000011.9:g.44286676C>T , CM000673.1:g.44286676C>T | GRCh37 |
NC_000011.8:g.44243252C>T | NCBI36 |
NG_015809.1:g.50041G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000652299.1:c.964G>A MANE Select | ENSP00000498217.1:p.Val322Met | |
ENST00000329255.3:c.964G>A | ENSP00000332744.3:p.Val322Met | |
NM_021926.3:c.964G>A | NP_068745.2:p.Val322Met | |
XM_011520265.1:c.442G>A | XP_011518567.1:p.Val148Met | |
XM_011520266.1:c.442G>A | XP_011518568.1:p.Val148Met | |
NM_021926.4:c.964G>A MANE Select | NP_068745.2:p.Val322Met |