Canonical Allele Identifier: CA983143387
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1912144325

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448975A>C , CM000679.2:g.33448975A>C GRCh38
NC_000017.10:g.31775993A>C , CM000679.1:g.31775993A>C GRCh37
NC_000017.9:g.28800106A>C NCBI36
NG_029763.1:g.712833T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.556-336908T>G ENSP00000352934.6:n.556-336908T>G
NM_001094.4:c.556-336908T>G NP_001085.2:n.556-336908T>G
NM_001094.5:c.556-336908T>G NP_001085.2:n.556-336908T>G