Canonical Allele Identifier: CA289878344
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs62057458
gnomAD v2: 17-32306486-C-T
gnomAD v3: 17-33979467-C-T
gnomAD v4: 17-33979467-C-T
MyVariant Identifiers: chr17:g.32306486C>T (hg19) chr17:g.33979467C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979467C>T , CM000679.2:g.33979467C>T GRCh38
NC_000017.10:g.32306486C>T , CM000679.1:g.32306486C>T GRCh37
NC_000017.9:g.29330599C>T NCBI36
NG_029763.1:g.182340G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176511G>A ENSP00000352934.6:n.555+176511G>A
NM_001094.4:c.555+176511G>A NP_001085.2:n.555+176511G>A
XR_001752840.1:n.404+7678G>A
NM_001094.5:c.555+176511G>A NP_001085.2:n.555+176511G>A
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