Canonical Allele Identifier: CA427349389
Gene:

Linked Data

dbSNP Id: rs1416828512
gnomAD v3: 2-88016372-G-A
gnomAD v4: 2-88016372-G-A
MyVariant Identifiers: chr2:g.88315891G>A (hg19) chr2:g.88016372G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016372G>A , CM000664.2:g.88016372G>A GRCh38
NC_000002.11:g.88315891G>A , CM000664.1:g.88315891G>A GRCh37
NC_000002.10:g.88097006G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.717G>A
XR_940336.3:n.717G>A
Search 100 bp 5'
Search 100 bp 3'