Canonical Allele Identifier: CA289878367
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs112909723
gnomAD v2: 17-32306711-C-G
gnomAD v3: 17-33979692-C-G
gnomAD v4: 17-33979692-C-G
MyVariant Identifiers: chr17:g.32306711C>G (hg19) chr17:g.33979692C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979692C>G , CM000679.2:g.33979692C>G GRCh38
NC_000017.10:g.32306711C>G , CM000679.1:g.32306711C>G GRCh37
NC_000017.9:g.29330824C>G NCBI36
NG_029763.1:g.182115G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176286G>C ENSP00000352934.6:n.555+176286G>C
NM_001094.4:c.555+176286G>C NP_001085.2:n.555+176286G>C
XR_001752840.1:n.404+7453G>C
NM_001094.5:c.555+176286G>C NP_001085.2:n.555+176286G>C
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