Canonical Allele Identifier: CA2256579705
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1912133040

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448730T>C , CM000679.2:g.33448730T>C GRCh38
NC_000017.10:g.31775748T>C , CM000679.1:g.31775748T>C GRCh37
NC_000017.9:g.28799861T>C NCBI36
NG_029763.1:g.713078A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336663A>G ENSP00000352934.6:n.556-336663A>G
NM_001094.4:c.556-336663A>G NP_001085.2:n.556-336663A>G
NM_001094.5:c.556-336663A>G NP_001085.2:n.556-336663A>G