Canonical Allele Identifier: CA625752014
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1353856943
gnomAD v2: 17-32306250-C-CA
gnomAD v3: 17-33979231-C-CA
gnomAD v4: 17-33979231-C-CA
MyVariant Identifiers: chr17:g.32306250_32306251insA (hg19) chr17:g.33979231_33979232insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979232dup , CM000679.2:g.33979232dup GRCh38
NC_000017.10:g.32306251dup , CM000679.1:g.32306251dup GRCh37
NC_000017.9:g.29330364dup NCBI36
NG_029763.1:g.182575dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176746dup ENSP00000352934.6:n.555+176746dup
NM_001094.4:c.555+176746dup NP_001085.2:n.555+176746dup
XR_001752840.1:n.404+7913dup
NM_001094.5:c.555+176746dup NP_001085.2:n.555+176746dup
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