Canonical Allele Identifier: CA2256404301
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs2092045280
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33066796T>G , CM000679.2:g.33066796T>G GRCh38
NC_000017.10:g.31393814T>G , CM000679.1:g.31393814T>G GRCh37
NC_000017.9:g.28417927T>G NCBI36
NG_029763.1:g.1095012A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225823.7:c.987+22067A>C MANE Select ENSP00000225823.2:n.987+22067A>C
ENST00000225823.6:c.987+22067A>C ENSP00000225823.2:n.987+22067A>C
ENST00000359872.6:c.834+22067A>C ENSP00000352934.6:n.834+22067A>C
ENST00000448983.1:n.392+22067A>C
NM_001094.4:c.834+22067A>C NP_001085.2:n.834+22067A>C
NM_183377.1:c.987+22067A>C NP_899233.1:n.987+22067A>C
NM_001094.5:c.834+22067A>C NP_001085.2:n.834+22067A>C
NM_183377.2:c.987+22067A>C MANE Select NP_899233.1:n.987+22067A>C
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