Canonical Allele Identifier: CA2256579662
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1912128807

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448632C>G , CM000679.2:g.33448632C>G GRCh38
NC_000017.10:g.31775650C>G , CM000679.1:g.31775650C>G GRCh37
NC_000017.9:g.28799763C>G NCBI36
NG_029763.1:g.713176G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.556-336565G>C ENSP00000352934.6:n.556-336565G>C
NM_001094.4:c.556-336565G>C NP_001085.2:n.556-336565G>C
NM_001094.5:c.556-336565G>C NP_001085.2:n.556-336565G>C