Canonical Allele Identifier: CA1691656449
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957863T= , CM000669.2:g.17957863T= GRCh38
NC_000007.13:g.17997486T= , CM000669.1:g.17997486T= GRCh37
NC_000007.12:g.17964011T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-807T=