HGVS | Genome Assembly |
---|---|
NC_000007.14:g.27095597C>T , CM000669.2:g.27095597C>T | GRCh38 |
NC_000007.13:g.27135216C>T , CM000669.1:g.27135216C>T | GRCh37 |
NC_000007.12:g.27101741C>T | NCBI36 |
NG_011813.1:g.5410G>A | |
NG_033087.1:g.4504C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643460.2:c.316G>A MANE Select | ENSP00000494260.2:p.Ala106Thr | |
ENST00000343060.4:c.316G>A | ENSP00000343246.4:p.Ala106Thr | |
ENST00000355633.5:c.316G>A | ENSP00000347851.5:p.Ala106Thr | |
NM_005522.4:c.316G>A | NP_005513.1:p.Ala106Thr | |
NM_153620.2:c.316G>A | NP_705873.2:p.Ala106Thr | |
NM_005522.5:c.316G>A MANE Select | NP_005513.2:p.Ala106Thr | |
NM_153620.3:c.316G>A | NP_705873.3:p.Ala106Thr |