Canonical Allele Identifier: CA289838399
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs11652874

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33643464C>G , CM000679.2:g.33643464C>G GRCh38
NC_000017.10:g.31970483C>G , CM000679.1:g.31970483C>G GRCh37
NC_000017.9:g.28994596C>G NCBI36
NG_029763.1:g.518343G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+512514G>C ENSP00000352934.6:n.555+512514G>C
NM_001094.4:c.555+512514G>C NP_001085.2:n.555+512514G>C
NM_001094.5:c.555+512514G>C NP_001085.2:n.555+512514G>C