Canonical Allele Identifier: CA2761911327
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558143A>C , CM000666.2:g.62558143A>C GRCh38
NC_000004.11:g.63423861A>C , CM000666.1:g.63423861A>C GRCh37
NC_000004.10:g.63106456A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5701A>C