Canonical Allele Identifier: CA728269035
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1399345048
MyVariant Identifiers: chr17:g.32306468C>T (hg19) chr17:g.33979449C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979449C>T , CM000679.2:g.33979449C>T GRCh38
NC_000017.10:g.32306468C>T , CM000679.1:g.32306468C>T GRCh37
NC_000017.9:g.29330581C>T NCBI36
NG_029763.1:g.182358G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176529G>A ENSP00000352934.6:n.555+176529G>A
NM_001094.4:c.555+176529G>A NP_001085.2:n.555+176529G>A
XR_001752840.1:n.404+7696G>A
NM_001094.5:c.555+176529G>A NP_001085.2:n.555+176529G>A
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