HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115033483A>G , CM000663.2:g.115033483A>G | GRCh38 |
NC_000001.10:g.115576104A>G , CM000663.1:g.115576104A>G | GRCh37 |
NC_000001.9:g.115377627A>G | NCBI36 |
NG_015891.1:g.8690A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256592.3:c.121A>G MANE Select | ENSP00000256592.1:p.Thr41Ala | |
ENST00000256592.2:c.121A>G | ENSP00000256592.1:p.Thr41Ala | |
ENST00000369517.1:c.121A>G | ENSP00000358530.1:p.Thr41Ala | |
NM_000549.4:c.121A>G | NP_000540.2:p.Thr41Ala | |
XM_011542065.1:c.121A>G | XP_011540367.1:p.Thr41Ala | |
XM_011542065.2:c.121A>G | XP_011540367.1:p.Thr41Ala | |
NM_000549.5:c.121A>G MANE Select | NP_000540.2:p.Thr41Ala |