HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127401111T>C , CM000670.2:g.127401111T>C | GRCh38 |
NC_000008.10:g.128413356T>C , CM000670.1:g.128413356T>C | GRCh37 |
NC_000008.9:g.128482538T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645438.1:c.-559-13777T>C (POU5F1B) | ENSP00000495779.1:n.-559-13777T>C | |
NR_109834.1:n.713T>C (CCAT2) | ||
NR_117100.1:n.1176+19718A>G (CASC8) |