HGVS | Genome Assembly |
---|---|
NC_000010.11:g.17129861A>T , CM000672.2:g.17129861A>T | GRCh38 |
NC_000010.10:g.17171860A>T , CM000672.1:g.17171860A>T | GRCh37 |
NC_000010.9:g.17211866A>T | NCBI36 |
NG_008967.1:g.4957T>A , LRG_540:g.4957T>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011519708.1:c.-96T>A | XP_011518010.1:n.-96T>A | |
XM_011519708.2:c.-96T>A | XP_011518010.1:n.-96T>A |