Canonical Allele Identifier: CA1462694300
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558272T= , CM000666.2:g.62558272T= GRCh38
NC_000004.11:g.63423990T= , CM000666.1:g.63423990T= GRCh37
NC_000004.10:g.63106585T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5572T=