Canonical Allele Identifier: CA1691656492
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957953C= , CM000669.2:g.17957953C= GRCh38
NC_000007.13:g.17997576C= , CM000669.1:g.17997576C= GRCh37
NC_000007.12:g.17964101C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-717C=