Canonical Allele Identifier: CA289815010
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs944218532
gnomAD v3: 17-33448718-A-C
gnomAD v4: 17-33448718-A-C
MyVariant Identifiers: chr17:g.31775736A>C (hg19) chr17:g.33448718A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448718A>C , CM000679.2:g.33448718A>C GRCh38
NC_000017.10:g.31775736A>C , CM000679.1:g.31775736A>C GRCh37
NC_000017.9:g.28799849A>C NCBI36
NG_029763.1:g.713090T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336651T>G ENSP00000352934.6:n.556-336651T>G
NM_001094.4:c.556-336651T>G NP_001085.2:n.556-336651T>G
NM_001094.5:c.556-336651T>G NP_001085.2:n.556-336651T>G
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