Canonical Allele Identifier: CA116433017
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.29040014T>G , CM000667.2:g.29040014T>G GRCh38
NC_000005.9:g.29040121T>G , CM000667.1:g.29040121T>G GRCh37
NC_000005.8:g.29075878T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742622.1:n.346-405A>C
XR_001742623.1:n.346-405A>C