Canonical Allele Identifier: CA983143313
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1912133822

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448741A>T , CM000679.2:g.33448741A>T GRCh38
NC_000017.10:g.31775759A>T , CM000679.1:g.31775759A>T GRCh37
NC_000017.9:g.28799872A>T NCBI36
NG_029763.1:g.713067T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336674T>A ENSP00000352934.6:n.556-336674T>A
NM_001094.4:c.556-336674T>A NP_001085.2:n.556-336674T>A
NM_001094.5:c.556-336674T>A NP_001085.2:n.556-336674T>A