Canonical Allele Identifier: CA2256404260
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1598260805
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33066681C>T , CM000679.2:g.33066681C>T GRCh38
NC_000017.10:g.31393699C>T , CM000679.1:g.31393699C>T GRCh37
NC_000017.9:g.28417812C>T NCBI36
NG_029763.1:g.1095127G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225823.7:c.987+22182G>A MANE Select ENSP00000225823.2:n.987+22182G>A
ENST00000225823.6:c.987+22182G>A ENSP00000225823.2:n.987+22182G>A
ENST00000359872.6:c.834+22182G>A ENSP00000352934.6:n.834+22182G>A
ENST00000448983.1:n.392+22182G>A
NM_001094.4:c.834+22182G>A NP_001085.2:n.834+22182G>A
NM_183377.1:c.987+22182G>A NP_899233.1:n.987+22182G>A
NM_001094.5:c.834+22182G>A NP_001085.2:n.834+22182G>A
NM_183377.2:c.987+22182G>A MANE Select NP_899233.1:n.987+22182G>A
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