HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114045105A>G , CM000672.2:g.114045105A>G | GRCh38 |
NC_000010.10:g.115804864A>G , CM000672.1:g.115804864A>G | GRCh37 |
NC_000010.9:g.115794854A>G | NCBI36 |
NG_012187.1:g.6059A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.973A>G MANE Select | ENSP00000358301.2:p.Thr325Ala | |
ENST00000369295.3:c.973A>G | ENSP00000358301.2:p.Thr325Ala | |
NM_000684.2:c.973A>G | NP_000675.1:p.Thr325Ala | |
NM_000684.3:c.973A>G MANE Select | NP_000675.1:p.Thr325Ala |