Canonical Allele Identifier: CA1695966091
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605797C= , CM000669.2:g.26605797C= GRCh38
NC_000007.13:g.26645416C= , CM000669.1:g.26645416C= GRCh37
NC_000007.12:g.26611941C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6427G=
XR_927131.2:n.1186-6427G=