Canonical Allele Identifier: CA1804700779
Community Standard Title: NC_000008.11:g.97154685T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97154685T= , CM000670.2:g.97154685T= GRCh38
NC_000008.10:g.98166913T= , CM000670.1:g.98166913T= GRCh37
NC_000008.9:g.98236089T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.472-201075A=
XR_928434.1:n.1748+4013T=
XR_928434.2:n.1770+4013T=
XR_928435.1:n.1748+4013T=