Canonical Allele Identifier: CA14491363
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1123025
gnomAD v2: 17-31775823-C-T
gnomAD v3: 17-33448805-C-T
gnomAD v4: 17-33448805-C-T
MyVariant Identifiers: chr17:g.31775823C>T (hg19) chr17:g.33448805C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448805C>T , CM000679.2:g.33448805C>T GRCh38
NC_000017.10:g.31775823C>T , CM000679.1:g.31775823C>T GRCh37
NC_000017.9:g.28799936C>T NCBI36
NG_029763.1:g.713003G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336738G>A ENSP00000352934.6:n.556-336738G>A
NM_001094.4:c.556-336738G>A NP_001085.2:n.556-336738G>A
NM_001094.5:c.556-336738G>A NP_001085.2:n.556-336738G>A
Search 100 bp 5'
Search 100 bp 3'