HGVS | Genome Assembly |
---|---|
NC_000001.11:g.168293219A>G , CM000663.2:g.168293219A>G | GRCh38 |
NC_000001.10:g.168262457A>G , CM000663.1:g.168262457A>G | GRCh37 |
NC_000001.9:g.166529081A>G | NCBI36 |
NG_008244.1:g.17180A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367821.8:c.544A>G MANE Select | ENSP00000356795.3:p.Thr182Ala | |
ENST00000367821.7:c.544A>G | ENSP00000356795.3:p.Thr182Ala | |
ENST00000431969.5:c.341A>G | ||
NM_005149.2:c.544A>G | NP_005140.1:p.Thr182Ala | |
NM_005149.3:c.544A>G MANE Select | NP_005140.1:p.Thr182Ala |