Canonical Allele Identifier: CA890088233
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs1261536819
MyVariant Identifiers: chr1:g.160007351T>G (hg19) chr1:g.160037561T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160037561T>G , CM000663.2:g.160037561T>G GRCh38
NC_000001.10:g.160007351T>G , CM000663.1:g.160007351T>G GRCh37
NC_000001.9:g.158273975T>G NCBI36
NG_016411.1:g.37611A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+4273A>C
ENST00000637644.1:c.487+4485A>C ENSP00000490282.1:n.487+4485A>C
ENST00000639408.1:c.587+2941A>C ENSP00000491635.1:n.587+2941A>C
ENST00000640914.1:c.224+2941A>C
ENST00000644903.1:c.*3832A>C MANE Select ENSP00000495557.1:n.*3832A>C
ENST00000368089.3:c.*3832A>C ENSP00000357068.3:n.*3832A>C
NM_002241.4:c.*3832A>C NP_002232.2:n.*3832A>C
NM_002241.5:c.*3832A>C MANE Select NP_002232.2:n.*3832A>C
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