Canonical Allele Identifier: CA1258276522
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637482T= , CM000664.2:g.67637482T= GRCh38
NC_000002.11:g.67864614T= , CM000664.1:g.67864614T= GRCh37
NC_000002.10:g.67718118T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13484A=