HGVS | Genome Assembly |
---|---|
NC_000009.12:g.37437011G>T , CM000671.2:g.37437011G>T | GRCh38 |
NC_000009.11:g.37437008G>T , CM000671.1:g.37437008G>T | GRCh37 |
NC_000009.10:g.37427008G>T | NCBI36 |
NG_008135.1:g.19302G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_017015320.2:c.946-400G>T | XP_016870809.1:n.946-400G>T | |
XM_017015321.2:c.866-400G>T | XP_016870810.1:n.866-400G>T | |
XM_017015323.2:c.544-400G>T | XP_016870812.1:n.544-400G>T | |
XM_024447716.1:c.1219-400G>T | XP_024303484.1:n.1219-400G>T | |
XM_024447717.1:c.1139-400G>T | XP_024303485.1:n.1139-400G>T | |
XR_002956828.1:n.1234-400G>T | ||
XR_002956829.1:n.1154-400G>T |