HGVS | Genome Assembly |
---|---|
NC_000010.11:g.17129853T>G , CM000672.2:g.17129853T>G | GRCh38 |
NC_000010.10:g.17171852T>G , CM000672.1:g.17171852T>G | GRCh37 |
NC_000010.9:g.17211858T>G | NCBI36 |
NG_008967.1:g.4965A>C , LRG_540:g.4965A>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_011519708.1:c.-88A>C | XP_011518010.1:n.-88A>C | |
XM_011519708.2:c.-88A>C | XP_011518010.1:n.-88A>C |