Canonical Allele Identifier: CA289815011
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs191021303
gnomAD v2: 17-31775749-C-A
gnomAD v3: 17-33448731-C-A
gnomAD v4: 17-33448731-C-A
MyVariant Identifiers: chr17:g.31775749C>A (hg19) chr17:g.33448731C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448731C>A , CM000679.2:g.33448731C>A GRCh38
NC_000017.10:g.31775749C>A , CM000679.1:g.31775749C>A GRCh37
NC_000017.9:g.28799862C>A NCBI36
NG_029763.1:g.713077G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.556-336664G>T ENSP00000352934.6:n.556-336664G>T
NM_001094.4:c.556-336664G>T NP_001085.2:n.556-336664G>T
NM_001094.5:c.556-336664G>T NP_001085.2:n.556-336664G>T
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