HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67932036C>T , CM000666.2:g.67932036C>T | GRCh38 |
NC_000004.11:g.68797754C>T , CM000666.1:g.68797754C>T | GRCh37 |
NC_000004.10:g.68480349C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000508048.6:c.277G>A MANE Select | ENSP00000426911.2:p.Ala93Thr | |
ENST00000334830.11:c.286G>A | ENSP00000334611.7:p.Ala96Thr | |
ENST00000396188.3:c.277G>A | ENSP00000379491.3:p.Ala93Thr | |
ENST00000508048.5:c.277G>A | ENSP00000426911.2:p.Ala93Thr | |
ENST00000513536.5:c.217G>A | ENSP00000427621.1:p.Ala73Thr | |
NM_001114387.1:c.277G>A | NP_001107859.1:p.Ala93Thr | |
NM_182606.3:c.286G>A | NP_872412.3:p.Ala96Thr | |
NM_001114387.2:c.277G>A MANE Select | NP_001107859.1:p.Ala93Thr | |
NM_182606.4:c.286G>A | NP_872412.3:p.Ala96Thr |