Canonical Allele Identifier: CA2761911342
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558490G>C , CM000666.2:g.62558490G>C GRCh38
NC_000004.11:g.63424208G>C , CM000666.1:g.63424208G>C GRCh37
NC_000004.10:g.63106803G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5354G>C