Canonical Allele Identifier: CA2256826608
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979352G= , CM000679.2:g.33979352G= GRCh38
NC_000017.10:g.32306371G= , CM000679.1:g.32306371G= GRCh37
NC_000017.9:g.29330484G= NCBI36
NG_029763.1:g.182455C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176626C= ENSP00000352934.6:n.555+176626C=
NM_001094.4:c.555+176626C= NP_001085.2:n.555+176626C=
XR_001752840.1:n.404+7793C=
NM_001094.5:c.555+176626C= NP_001085.2:n.555+176626C=