Canonical Allele Identifier: CA2256826683
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905530352
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979493C>T , CM000679.2:g.33979493C>T GRCh38
NC_000017.10:g.32306512C>T , CM000679.1:g.32306512C>T GRCh37
NC_000017.9:g.29330625C>T NCBI36
NG_029763.1:g.182314G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176485G>A ENSP00000352934.6:n.555+176485G>A
NM_001094.4:c.555+176485G>A NP_001085.2:n.555+176485G>A
XR_001752840.1:n.404+7652G>A
NM_001094.5:c.555+176485G>A NP_001085.2:n.555+176485G>A
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