Canonical Allele Identifier: CA1462694277
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558230G= , CM000666.2:g.62558230G= GRCh38
NC_000004.11:g.63423948G= , CM000666.1:g.63423948G= GRCh37
NC_000004.10:g.63106543G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5614G=