HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37217308A>T , CM000684.2:g.37217308A>T | GRCh38 |
NC_000022.10:g.37613348A>T , CM000684.1:g.37613348A>T | GRCh37 |
NC_000022.9:g.35943294A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_005261721.3:c.-37+3099T>A | XP_005261778.1:n.-37+3099T>A | |
XM_011530349.1:c.-694-1420T>A | XP_011528651.1:n.-694-1420T>A | |
XM_005261721.4:c.-37+3099T>A | XP_005261778.1:n.-37+3099T>A | |
XM_011530349.2:c.-694-1420T>A | XP_011528651.1:n.-694-1420T>A | |
XM_017028924.1:c.-437-1420T>A | XP_016884413.1:n.-437-1420T>A |