Canonical Allele Identifier: CA2581169181
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857024G>C , CM000676.2:g.50857024G>C GRCh38
NC_000014.8:g.51323742G>C , CM000676.1:g.51323742G>C GRCh37
NC_000014.7:g.50393492G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1074C>G
XR_943848.2:n.643+1074C>G