Canonical Allele Identifier: CA1816081229
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395885C= , CM000670.2:g.122395885C= GRCh38
NC_000008.10:g.123408124C= , CM000670.1:g.123408124C= GRCh37
NC_000008.9:g.123477305C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3287G=
XR_928599.3:n.152+3287G=