HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127401361G= , CM000670.2:g.127401361G= | GRCh38 |
NC_000008.10:g.128413606G= , CM000670.1:g.128413606G= | GRCh37 |
NC_000008.9:g.128482788G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645438.1:c.-559-13527G= (POU5F1B) | ENSP00000495779.1:n.-559-13527G= | |
NR_109834.1:n.963G= (CCAT2) | ||
NR_117100.1:n.1176+19468C= (CASC8) |