Canonical Allele Identifier: CA51878293
Gene:

Linked Data

dbSNP Id: rs533018238
gnomAD v2: 2-88315705-T-C
gnomAD v3: 2-88016186-T-C
gnomAD v4: 2-88016186-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016186T>C , CM000664.2:g.88016186T>C GRCh38
NC_000002.11:g.88315705T>C , CM000664.1:g.88315705T>C GRCh37
NC_000002.10:g.88096820T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.531T>C
XR_940336.3:n.531T>C