Canonical Allele Identifier: CA669472914
Gene:

Linked Data

dbSNP Id: rs1284298149

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697667A>C , CM000672.2:g.8697667A>C GRCh38
NC_000010.10:g.8739630A>C , CM000672.1:g.8739630A>C GRCh37
NC_000010.9:g.8779636A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27866T>G