HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127401119G>T , CM000670.2:g.127401119G>T | GRCh38 |
NC_000008.10:g.128413364G>T , CM000670.1:g.128413364G>T | GRCh37 |
NC_000008.9:g.128482546G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645438.1:c.-559-13769G>T (POU5F1B) | ENSP00000495779.1:n.-559-13769G>T | |
NR_109834.1:n.721G>T (CCAT2) | ||
NR_117100.1:n.1176+19710C>A (CASC8) |