Canonical Allele Identifier: CA1059430042
Gene:

Linked Data

dbSNP Id: rs1711590266
gnomAD v3: 4-12578264-C-G
gnomAD v4: 4-12578264-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578264C>G , CM000666.2:g.12578264C>G GRCh38
NC_000004.11:g.12579888C>G , CM000666.1:g.12579888C>G GRCh37
NC_000004.10:g.12188986C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31078G>C
XR_001741374.1:n.254+44391G>C
XR_925406.3:n.140+31078G>C