Canonical Allele Identifier: CA1800979696
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981082T= , CM000670.2:g.88981082T= GRCh38
NC_000008.10:g.89993311T= , CM000670.1:g.89993311T= GRCh37
NC_000008.9:g.90062427T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99021A=