Canonical Allele Identifier: CA2256826590
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979308A= , CM000679.2:g.33979308A= GRCh38
NC_000017.10:g.32306327A= , CM000679.1:g.32306327A= GRCh37
NC_000017.9:g.29330440A= NCBI36
NG_029763.1:g.182499T=

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176670T= ENSP00000352934.6:n.555+176670T=
NM_001094.4:c.555+176670T= NP_001085.2:n.555+176670T=
XR_001752840.1:n.404+7837T=
NM_001094.5:c.555+176670T= NP_001085.2:n.555+176670T=