Canonical Allele Identifier: CA983177639
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905520088

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979320G>C , CM000679.2:g.33979320G>C GRCh38
NC_000017.10:g.32306339G>C , CM000679.1:g.32306339G>C GRCh37
NC_000017.9:g.29330452G>C NCBI36
NG_029763.1:g.182487C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176658C>G ENSP00000352934.6:n.555+176658C>G
NM_001094.4:c.555+176658C>G NP_001085.2:n.555+176658C>G
XR_001752840.1:n.404+7825C>G
NM_001094.5:c.555+176658C>G NP_001085.2:n.555+176658C>G