Canonical Allele Identifier: CA427349486
Gene:

Linked Data

dbSNP Id: rs78243397
gnomAD v3: 2-88016415-A-C
gnomAD v4: 2-88016415-A-C
MyVariant Identifiers: chr2:g.88315934A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016415A>C , CM000664.2:g.88016415A>C GRCh38
NC_000002.11:g.88315934A>C , CM000664.1:g.88315934A>C GRCh37
NC_000002.10:g.88097049A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.760A>C
XR_940336.3:n.760A>C