Canonical Allele Identifier: CA289815022

Gene: ASIC2

Linked Data

• dbSNP Id: rs983307591
• gnomAD v3: 17-33448820-A-G
• gnomAD v4: 17-33448820-A-G
• MyVariant Identifiers: chr17:g.31775838A>G (hg19) ; chr17:g.33448820A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33448820A>G , CM000679.2:g.33448820A>G	GRCh38
NC_000017.10:g.31775838A>G , CM000679.1:g.31775838A>G	GRCh37
NC_000017.9:g.28799951A>G	NCBI36
NG_029763.1:g.712988T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359872.6:c.556-336753T>C	ENSP00000352934.6:n.556-336753T>C
NM_001094.4:c.556-336753T>C	NP_001085.2:n.556-336753T>C
NM_001094.5:c.556-336753T>C	NP_001085.2:n.556-336753T>C