Canonical Allele Identifier: CA2256826604
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905520761

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979333T>C , CM000679.2:g.33979333T>C GRCh38
NC_000017.10:g.32306352T>C , CM000679.1:g.32306352T>C GRCh37
NC_000017.9:g.29330465T>C NCBI36
NG_029763.1:g.182474A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176645A>G ENSP00000352934.6:n.555+176645A>G
NM_001094.4:c.555+176645A>G NP_001085.2:n.555+176645A>G
XR_001752840.1:n.404+7812A>G
NM_001094.5:c.555+176645A>G NP_001085.2:n.555+176645A>G