Canonical Allele Identifier: CA427349534
Gene:

Linked Data

dbSNP Id: rs765721547
gnomAD v2: 2-88315956-T-G
gnomAD v3: 2-88016437-T-G
gnomAD v4: 2-88016437-T-G
MyVariant Identifiers: chr2:g.88315956T>G (hg19) chr2:g.88016437T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016437T>G , CM000664.2:g.88016437T>G GRCh38
NC_000002.11:g.88315956T>G , CM000664.1:g.88315956T>G GRCh37
NC_000002.10:g.88097071T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.782T>G
XR_940336.3:n.782T>G
Search 100 bp 5'
Search 100 bp 3'