Canonical Allele Identifier: CA1800979999
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981282G= , CM000670.2:g.88981282G= GRCh38
NC_000008.10:g.89993511G= , CM000670.1:g.89993511G= GRCh37
NC_000008.9:g.90062627G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99221C=