Canonical Allele Identifier: CA728268865
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1361002573
gnomAD v3: 17-33979285-A-AG
gnomAD v4: 17-33979285-A-AG
MyVariant Identifiers: chr17:g.32306304_32306305insG (hg19) chr17:g.33979285_33979286insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979286dup , CM000679.2:g.33979286dup GRCh38
NC_000017.10:g.32306305dup , CM000679.1:g.32306305dup GRCh37
NC_000017.9:g.29330418dup NCBI36
NG_029763.1:g.182521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176692dup ENSP00000352934.6:n.555+176692dup
NM_001094.4:c.555+176692dup NP_001085.2:n.555+176692dup
XR_001752840.1:n.404+7859dup
NM_001094.5:c.555+176692dup NP_001085.2:n.555+176692dup
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