Canonical Allele Identifier: CA1695631829
Community Standard Title: NC_000007.14:g.25862019G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25862019G= , CM000669.2:g.25862019G= GRCh38
NC_000007.13:g.25901639G= , CM000669.1:g.25901639G= GRCh37
NC_000007.12:g.25868164G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927109.1:n.122+125C=