Canonical Allele Identifier: CA289897632
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs9901756

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34137135A>C , CM000679.2:g.34137135A>C GRCh38
NC_000017.10:g.32464154A>C , CM000679.1:g.32464154A>C GRCh37
NC_000017.9:g.29488267A>C NCBI36
NG_029763.1:g.24672T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+18843T>G ENSP00000352934.6:n.555+18843T>G
NM_001094.4:c.555+18843T>G NP_001085.2:n.555+18843T>G
NM_001094.5:c.555+18843T>G NP_001085.2:n.555+18843T>G