Canonical Allele Identifier: CA427349452
Gene:

Linked Data

gnomAD v4: 2-88016396-T-A
MyVariant Identifiers: chr2:g.88315915T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016396T>A , CM000664.2:g.88016396T>A GRCh38
NC_000002.11:g.88315915T>A , CM000664.1:g.88315915T>A GRCh37
NC_000002.10:g.88097030T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.741T>A
XR_940336.3:n.741T>A
Search 100 bp 5'
Search 100 bp 3'