HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174794A>G , CM000674.2:g.21174794A>G | GRCh38 |
NC_000012.11:g.21327728A>G , CM000674.1:g.21327728A>G | GRCh37 |
NC_000012.10:g.21218995A>G | NCBI36 |
NG_011745.1:g.48601A>G , LRG_1022:g.48601A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.359+85A>G MANE Select | ENSP00000256958.2:n.359+85A>G | |
ENST00000256958.2:c.359+85A>G | ENSP00000256958.2:n.359+85A>G | |
ENST00000543498.5:c.426-1982A>G | ||
NM_006446.4:c.359+85A>G , LRG_1022t1:c.359+85A>G | NP_006437.3:n.359+85A>G | |
NM_006446.5:c.359+85A>G MANE Select | NP_006437.3:n.359+85A>G |