HGVS | Genome Assembly |
---|---|
NC_000011.10:g.34446099A>G , CM000673.2:g.34446099A>G | GRCh38 |
NC_000011.9:g.34467646A>G , CM000673.1:g.34467646A>G | GRCh37 |
NC_000011.8:g.34424222A>G | NCBI36 |
NG_013339.1:g.12175A>G | |
NG_013339.2:g.12175A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000241052.5:c.67-3093A>G MANE Select | ENSP00000241052.4:n.67-3093A>G | |
ENST00000241052.4:c.67-3093A>G | ENSP00000241052.4:n.67-3093A>G | |
NM_001752.3:c.67-3093A>G | NP_001743.1:n.67-3093A>G | |
NM_001752.4:c.67-3093A>G MANE Select | NP_001743.1:n.67-3093A>G |