Canonical Allele Identifier: CA2256826657
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979447T= , CM000679.2:g.33979447T= GRCh38
NC_000017.10:g.32306466T= , CM000679.1:g.32306466T= GRCh37
NC_000017.9:g.29330579T= NCBI36
NG_029763.1:g.182360A=

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176531A= ENSP00000352934.6:n.555+176531A=
NM_001094.4:c.555+176531A= NP_001085.2:n.555+176531A=
XR_001752840.1:n.404+7698A=
NM_001094.5:c.555+176531A= NP_001085.2:n.555+176531A=