Canonical Allele Identifier: CA2761911338
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558405C>T , CM000666.2:g.62558405C>T GRCh38
NC_000004.11:g.63424123C>T , CM000666.1:g.63424123C>T GRCh37
NC_000004.10:g.63106718C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5439C>T