Canonical Allele Identifier: CA1695966151
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605917A= , CM000669.2:g.26605917A= GRCh38
NC_000007.13:g.26645536A= , CM000669.1:g.26645536A= GRCh37
NC_000007.12:g.26612061A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6547T=
XR_927131.2:n.1186-6547T=