HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780518T>G , CM000672.2:g.94780518T>G | GRCh38 |
NC_000010.10:g.96540275T>G , CM000672.1:g.96540275T>G | GRCh37 |
NC_000010.9:g.96530265T>G | NCBI36 |
NG_008384.2:g.22813T>G | |
NG_008384.3:g.22838T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.501T>G MANE Select | ENSP00000360372.3:p.Thr167= | |
ENST00000645461.1:n.1554T>G | ||
ENST00000371321.7:c.501T>G | ENSP00000360372.3:p.Thr167= | |
ENST00000464755.1:c.1264T>G | ENSP00000483243.1:n.1264T>G | |
NM_000769.2:c.501T>G | NP_000760.1:p.Thr167= | |
NM_000769.4:c.501T>G MANE Select | NP_000760.1:p.Thr167= |