Canonical Allele Identifier: CA728214269
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1193902025
gnomAD v3: 17-33448713-C-G
gnomAD v4: 17-33448713-C-G
MyVariant Identifiers: chr17:g.31775731C>G (hg19) chr17:g.33448713C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448713C>G , CM000679.2:g.33448713C>G GRCh38
NC_000017.10:g.31775731C>G , CM000679.1:g.31775731C>G GRCh37
NC_000017.9:g.28799844C>G NCBI36
NG_029763.1:g.713095G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336646G>C ENSP00000352934.6:n.556-336646G>C
NM_001094.4:c.556-336646G>C NP_001085.2:n.556-336646G>C
NM_001094.5:c.556-336646G>C NP_001085.2:n.556-336646G>C
Search 100 bp 5'
Search 100 bp 3'