Canonical Allele Identifier: CA983154385
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1906644999
gnomAD v3: 17-33643407-C-T
gnomAD v4: 17-33643407-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33643407C>T , CM000679.2:g.33643407C>T GRCh38
NC_000017.10:g.31970426C>T , CM000679.1:g.31970426C>T GRCh37
NC_000017.9:g.28994539C>T NCBI36
NG_029763.1:g.518400G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+512571G>A ENSP00000352934.6:n.555+512571G>A
NM_001094.4:c.555+512571G>A NP_001085.2:n.555+512571G>A
NM_001094.5:c.555+512571G>A NP_001085.2:n.555+512571G>A
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