Canonical Allele Identifier: CA289878337
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs986049286
MyVariant Identifiers: chr17:g.32306433C>A (hg19) chr17:g.33979414C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979414C>A , CM000679.2:g.33979414C>A GRCh38
NC_000017.10:g.32306433C>A , CM000679.1:g.32306433C>A GRCh37
NC_000017.9:g.29330546C>A NCBI36
NG_029763.1:g.182393G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176564G>T ENSP00000352934.6:n.555+176564G>T
NM_001094.4:c.555+176564G>T NP_001085.2:n.555+176564G>T
XR_001752840.1:n.404+7731G>T
NM_001094.5:c.555+176564G>T NP_001085.2:n.555+176564G>T
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