HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852943T>G , CM000672.2:g.94852943T>G | GRCh38 |
NC_000010.10:g.96612700T>G , CM000672.1:g.96612700T>G | GRCh37 |
NC_000010.9:g.96602690T>G | NCBI36 |
NG_008384.2:g.95238T>G | |
NG_008384.3:g.95263T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.*29T>G MANE Select | ENSP00000360372.3:n.*29T>G | |
ENST00000645461.1:n.2413T>G | ||
ENST00000371321.7:c.*29T>G | ENSP00000360372.3:n.*29T>G | |
ENST00000464755.1:c.2265T>G | ENSP00000483243.1:n.2265T>G | |
NM_000769.2:c.*29T>G | NP_000760.1:n.*29T>G | |
NM_000769.4:c.*29T>G MANE Select | NP_000760.1:n.*29T>G |