Canonical Allele Identifier: CA1140226713
Community Standard Title: NC_000001.11:g.88186088C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.88186088C= , CM000663.2:g.88186088C= GRCh38
NC_000001.10:g.88651771C= , CM000663.1:g.88651771C= GRCh37
NC_000001.9:g.88424359C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947571.1:n.314-9900G=