HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1401446C>T , CM000681.2:g.1401446C>T | GRCh38 |
NC_000019.9:g.1401445C>T , CM000681.1:g.1401445C>T | GRCh37 |
NC_000019.8:g.1352445C>T | NCBI36 |
NG_009785.1:g.5108G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252288.8:c.31G>A MANE Select | ENSP00000252288.1:p.Ala11Thr | |
ENST00000447102.8:c.31G>A | ENSP00000403536.2:p.Ala11Thr | |
ENST00000640762.1:c.31G>A | ENSP00000492031.1:p.Ala11Thr | |
ENST00000252288.6:c.31G>A | ENSP00000252288.1:p.Ala11Thr | |
ENST00000447102.7:c.31G>A | ENSP00000403536.2:p.Ala11Thr | |
NM_000156.5:c.31G>A | NP_000147.1:p.Ala11Thr | |
NM_138924.2:c.31G>A | NP_620279.1:p.Ala11Thr | |
NM_000156.6:c.31G>A MANE Select | NP_000147.1:p.Ala11Thr | |
NM_138924.3:c.31G>A | NP_620279.1:p.Ala11Thr |