Canonical Allele Identifier: CA1800979793
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981130A= , CM000670.2:g.88981130A= GRCh38
NC_000008.10:g.89993359A= , CM000670.1:g.89993359A= GRCh37
NC_000008.9:g.90062475A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99069T=