HGVS | Genome Assembly |
---|---|
NC_000001.11:g.35561155C>G , CM000663.2:g.35561155C>G | GRCh38 |
NC_000001.10:g.36026756C>G , CM000663.1:g.36026756C>G | GRCh37 |
NC_000001.9:g.35799343C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373243.7:c.1004C>G MANE Select | ENSP00000362340.2:p.Thr335Ser | |
ENST00000356090.8:c.1004C>G | ENSP00000348394.4:p.Thr335Ser | |
ENST00000373243.6:c.1004C>G | ENSP00000362340.2:p.Thr335Ser | |
ENST00000373253.7:c.953C>G | ENSP00000362350.3:p.Thr318Ser | |
NM_001014839.1:c.1004C>G | NP_001014839.1:p.Thr335Ser | |
NM_001014841.1:c.953C>G | NP_001014841.1:p.Thr318Ser | |
NM_014284.2:c.1004C>G | NP_055099.1:p.Thr335Ser | |
NM_014284.3:c.1004C>G MANE Select | NP_055099.1:p.Thr335Ser | |
NM_001014839.2:c.1004C>G | NP_001014839.1:p.Thr335Ser | |
NM_001014841.2:c.953C>G | NP_001014841.1:p.Thr318Ser |