Canonical Allele Identifier: CA11932699
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.73136209C>G , CM000667.2:g.73136209C>G GRCh38
NC_000005.9:g.72432036C>G , CM000667.1:g.72432036C>G GRCh37
NC_000005.8:g.72467792C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948469.1:n.273-3926G>C
NR_134252.1:n.174-3926G>C