Canonical Allele Identifier: CA1259578682
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70438512C= , CM000664.2:g.70438512C= GRCh38
NC_000002.11:g.70665644C= , CM000664.1:g.70665644C= GRCh37
NC_000002.10:g.70519152C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940229.1:n.230-2788C=