Canonical Allele Identifier: CA1757932380
Gene:

Linked Data

dbSNP Id: rs1660776702

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2180509G>T , CM000670.2:g.2180509G>T GRCh38
NC_000008.9:g.2116119G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941356.1:n.112-12426G>T
XR_941355.2:n.133-3515G>T
XR_941356.2:n.133-12426G>T