Canonical Allele Identifier: CA51878292
Gene:

Linked Data

dbSNP Id: rs369516133
gnomAD v2: 2-88315699-C-G
gnomAD v3: 2-88016180-C-G
gnomAD v4: 2-88016180-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016180C>G , CM000664.2:g.88016180C>G GRCh38
NC_000002.11:g.88315699C>G , CM000664.1:g.88315699C>G GRCh37
NC_000002.10:g.88096814C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.525C>G
XR_940336.3:n.525C>G