Canonical Allele Identifier: CA728292362
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs116908816

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34095680G>C , CM000679.2:g.34095680G>C GRCh38
NC_000017.10:g.32422699G>C , CM000679.1:g.32422699G>C GRCh37
NC_000017.9:g.29446812G>C NCBI36
NG_029763.1:g.66127C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+60298C>G ENSP00000352934.6:n.555+60298C>G
NM_001094.4:c.555+60298C>G NP_001085.2:n.555+60298C>G
XR_001752835.1:n.673-1647C>G
XR_002958157.1:n.643-1647C>G
NM_001094.5:c.555+60298C>G NP_001085.2:n.555+60298C>G