Canonical Allele Identifier: CA1462694298
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558267C= , CM000666.2:g.62558267C= GRCh38
NC_000004.11:g.63423985C= , CM000666.1:g.63423985C= GRCh37
NC_000004.10:g.63106580C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5577C=