Canonical Allele Identifier: CA728269142
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1338145289
MyVariant Identifiers: chr17:g.32306603A>G (hg19) chr17:g.33979584A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979584A>G , CM000679.2:g.33979584A>G GRCh38
NC_000017.10:g.32306603A>G , CM000679.1:g.32306603A>G GRCh37
NC_000017.9:g.29330716A>G NCBI36
NG_029763.1:g.182223T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176394T>C ENSP00000352934.6:n.555+176394T>C
NM_001094.4:c.555+176394T>C NP_001085.2:n.555+176394T>C
XR_001752840.1:n.404+7561T>C
NM_001094.5:c.555+176394T>C NP_001085.2:n.555+176394T>C
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