HGVS | Genome Assembly |
---|---|
NC_000009.12:g.37436998T>C , CM000671.2:g.37436998T>C | GRCh38 |
NC_000009.11:g.37436995T>C , CM000671.1:g.37436995T>C | GRCh37 |
NC_000009.10:g.37426995T>C | NCBI36 |
NG_008135.1:g.19289T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_017015320.2:c.946-413T>C | XP_016870809.1:n.946-413T>C | |
XM_017015321.2:c.866-413T>C | XP_016870810.1:n.866-413T>C | |
XM_017015323.2:c.544-413T>C | XP_016870812.1:n.544-413T>C | |
XM_024447716.1:c.1219-413T>C | XP_024303484.1:n.1219-413T>C | |
XM_024447717.1:c.1139-413T>C | XP_024303485.1:n.1139-413T>C | |
XR_002956828.1:n.1234-413T>C | ||
XR_002956829.1:n.1154-413T>C |