Canonical Allele Identifier: CA1695966082
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605765A= , CM000669.2:g.26605765A= GRCh38
NC_000007.13:g.26645384A= , CM000669.1:g.26645384A= GRCh37
NC_000007.12:g.26611909A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6395T=
XR_927131.2:n.1186-6395T=