Canonical Allele Identifier: CA289878332
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs915467133
gnomAD v3: 17-33979374-A-G
gnomAD v4: 17-33979374-A-G
MyVariant Identifiers: chr17:g.32306393A>G (hg19) chr17:g.33979374A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979374A>G , CM000679.2:g.33979374A>G GRCh38
NC_000017.10:g.32306393A>G , CM000679.1:g.32306393A>G GRCh37
NC_000017.9:g.29330506A>G NCBI36
NG_029763.1:g.182433T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176604T>C ENSP00000352934.6:n.555+176604T>C
NM_001094.4:c.555+176604T>C NP_001085.2:n.555+176604T>C
XR_001752840.1:n.404+7771T>C
NM_001094.5:c.555+176604T>C NP_001085.2:n.555+176604T>C
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