Canonical Allele Identifier: CA728269089
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1194780456

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979485A>C , CM000679.2:g.33979485A>C GRCh38
NC_000017.10:g.32306504A>C , CM000679.1:g.32306504A>C GRCh37
NC_000017.9:g.29330617A>C NCBI36
NG_029763.1:g.182322T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176493T>G ENSP00000352934.6:n.555+176493T>G
NM_001094.4:c.555+176493T>G NP_001085.2:n.555+176493T>G
XR_001752840.1:n.404+7660T>G
NM_001094.5:c.555+176493T>G NP_001085.2:n.555+176493T>G