HGVS | Genome Assembly |
---|---|
NC_000012.12:g.55996852A>T , CM000674.2:g.55996852A>T | GRCh38 |
NC_000012.11:g.56390636A>T , CM000674.1:g.56390636A>T | GRCh37 |
NC_000012.10:g.54676903A>T | NCBI36 |
NG_008136.1:g.4594A>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_017019905.2:c.-775A>T | XP_016875394.1:n.-775A>T | |
XM_017019907.2:c.-865A>T | XP_016875396.1:n.-865A>T | |
XM_024449167.1:c.-649A>T | XP_024304935.1:n.-649A>T |