Canonical Allele Identifier: CA185736831

Linked Data

dbSNP Id: rs776563023
MyVariant Identifiers: chr8:g.127400835C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400835C>A , CM000670.2:g.127400835C>A GRCh38
NC_000008.10:g.128413080C>A , CM000670.1:g.128413080C>A GRCh37
NC_000008.9:g.128482262C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-14053C>A (POU5F1B) ENSP00000495779.1:n.-559-14053C>A
NR_109834.1:n.437C>A (CCAT2)
NR_117100.1:n.1176+19994G>T (CASC8)