Canonical Allele Identifier: CA1462694372
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558448C= , CM000666.2:g.62558448C= GRCh38
NC_000004.11:g.63424166C= , CM000666.1:g.63424166C= GRCh37
NC_000004.10:g.63106761C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5396C=