Canonical Allele Identifier: CA289815034
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs911645313
gnomAD v3: 17-33448913-A-T
gnomAD v4: 17-33448913-A-T
MyVariant Identifiers: chr17:g.31775931A>T (hg19) chr17:g.33448913A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448913A>T , CM000679.2:g.33448913A>T GRCh38
NC_000017.10:g.31775931A>T , CM000679.1:g.31775931A>T GRCh37
NC_000017.9:g.28800044A>T NCBI36
NG_029763.1:g.712895T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.556-336846T>A ENSP00000352934.6:n.556-336846T>A
NM_001094.4:c.556-336846T>A NP_001085.2:n.556-336846T>A
NM_001094.5:c.556-336846T>A NP_001085.2:n.556-336846T>A
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