HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149925938C>T , CM000663.2:g.149925938C>T | GRCh38 |
NC_000001.10:g.149897830C>T , CM000663.1:g.149897830C>T | GRCh37 |
NC_000001.9:g.148164454C>T | NCBI36 |
NG_032777.1:g.7315G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.811G>A MANE Select | ENSP00000271628.8:p.Ala271Thr | |
ENST00000271628.8:c.811G>A | ENSP00000271628.8:p.Ala271Thr | |
NM_005850.4:c.811G>A | NP_005841.1:p.Ala271Thr | |
NM_005850.5:c.811G>A MANE Select | NP_005841.1:p.Ala271Thr |