Canonical Allele Identifier: CA2256826774
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905542135
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979704T>G , CM000679.2:g.33979704T>G GRCh38
NC_000017.10:g.32306723T>G , CM000679.1:g.32306723T>G GRCh37
NC_000017.9:g.29330836T>G NCBI36
NG_029763.1:g.182103A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176274A>C ENSP00000352934.6:n.555+176274A>C
NM_001094.4:c.555+176274A>C NP_001085.2:n.555+176274A>C
XR_001752840.1:n.404+7441A>C
NM_001094.5:c.555+176274A>C NP_001085.2:n.555+176274A>C
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