HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32644464A>G , CM000668.2:g.32644464A>G | GRCh38 |
NC_000006.11:g.32612241A>G , CM000668.1:g.32612241A>G | GRCh37 |
NC_000006.10:g.32720219A>G | NCBI36 |
NG_032876.1:g.12059A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460633.1:n.2852A>G | ||
XM_006715079.2:c.613+2211A>G | XP_006715142.1:n.613+2211A>G | |
XM_006715079.4:c.613+2211A>G | XP_006715142.1:n.613+2211A>G |