Canonical Allele Identifier: CA1963543688
Gene:

Genomic Alleles

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

Transcript Alleles

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