Canonical Allele Identifier: CA16538361
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1123024
gnomAD v2: 17-31775861-C-T
gnomAD v3: 17-33448843-C-T
gnomAD v4: 17-33448843-C-T
MyVariant Identifiers: chr17:g.31775861C>T (hg19) chr17:g.33448843C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448843C>T , CM000679.2:g.33448843C>T GRCh38
NC_000017.10:g.31775861C>T , CM000679.1:g.31775861C>T GRCh37
NC_000017.9:g.28799974C>T NCBI36
NG_029763.1:g.712965G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336776G>A ENSP00000352934.6:n.556-336776G>A
NM_001094.4:c.556-336776G>A NP_001085.2:n.556-336776G>A
NM_001094.5:c.556-336776G>A NP_001085.2:n.556-336776G>A
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