HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102481791A>G , CM000674.2:g.102481791A>G | GRCh38 |
NC_000012.11:g.102875569A>G , CM000674.1:g.102875569A>G | GRCh37 |
NC_000012.10:g.101399699A>G | NCBI36 |
NG_011713.1:g.3810T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_017019259.1:c.26T>C | XP_016874748.1:p.Val9Ala | |
XM_017019262.2:c.26T>C | XP_016874751.1:p.Val9Ala | |
XM_017019263.2:c.26T>C | XP_016874752.1:p.Val9Ala |