Canonical Allele Identifier: CA894254650
Gene:

Linked Data

dbSNP Id: rs1172652497
gnomAD v3: 2-88016337-T-C
gnomAD v4: 2-88016337-T-C
MyVariant Identifiers: chr2:g.88315856T>C (hg19) chr2:g.88016337T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016337T>C , CM000664.2:g.88016337T>C GRCh38
NC_000002.11:g.88315856T>C , CM000664.1:g.88315856T>C GRCh37
NC_000002.10:g.88096971T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.682T>C
XR_940336.3:n.682T>C
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Search 100 bp 3'