HGVS | Genome Assembly |
---|---|
NC_000009.12:g.37437042T>G , CM000671.2:g.37437042T>G | GRCh38 |
NC_000009.11:g.37437039T>G , CM000671.1:g.37437039T>G | GRCh37 |
NC_000009.10:g.37427039T>G | NCBI36 |
NG_008135.1:g.19333T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_017015320.2:c.946-369T>G | XP_016870809.1:n.946-369T>G | |
XM_017015321.2:c.866-369T>G | XP_016870810.1:n.866-369T>G | |
XM_017015323.2:c.544-369T>G | XP_016870812.1:n.544-369T>G | |
XM_024447716.1:c.1219-369T>G | XP_024303484.1:n.1219-369T>G | |
XM_024447717.1:c.1139-369T>G | XP_024303485.1:n.1139-369T>G | |
XR_002956828.1:n.1234-369T>G | ||
XR_002956829.1:n.1154-369T>G |