Canonical Allele Identifier: CA728268879
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1468607631
gnomAD v3: 17-33979307-CA-C
gnomAD v4: 17-33979307-CA-C
MyVariant Identifiers: chr17:g.32306327del (hg19) chr17:g.33979308del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979308del , CM000679.2:g.33979308del GRCh38
NC_000017.10:g.32306327del , CM000679.1:g.32306327del GRCh37
NC_000017.9:g.29330440del NCBI36
NG_029763.1:g.182499del

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176670del ENSP00000352934.6:n.555+176670del
NM_001094.4:c.555+176670del NP_001085.2:n.555+176670del
XR_001752840.1:n.404+7837del
NM_001094.5:c.555+176670del NP_001085.2:n.555+176670del
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