Canonical Allele Identifier: CA2072411556
Gene:

Linked Data

dbSNP Id: rs934949853

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529701C>G , CM000674.2:g.131529701C>G GRCh38
NC_000012.11:g.132014246C>G , CM000674.1:g.132014246C>G GRCh37
NC_000012.10:g.130580199C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+74G>C
XR_001749407.2:n.1067+74G>C