Canonical Allele Identifier: CA675884880
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35071523A>T , CM000673.2:g.35071523A>T GRCh38
NC_000011.9:g.35093070A>T , CM000673.1:g.35093070A>T GRCh37
NC_000011.8:g.35049646A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748182.1:n.41+2394T>A