Canonical Allele Identifier: CA856659511
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89329957A>T , CM000670.2:g.89329957A>T GRCh38
NC_000008.10:g.90342186A>T , CM000670.1:g.90342186A>T GRCh37
NC_000008.9:g.90411302A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956667.1:n.178+88087T>A