Canonical Allele Identifier: CA5902264

Gene: KCNJ11

Linked Data

• dbSNP Id: rs780169484
• ExAC: 11:17408970 G / C
• gnomAD v2: 11-17408970-G-C
• gnomAD v4: 11-17387423-G-C
• MyVariant Identifiers: chr11:g.17408970G>C (hg19) ; chr11:g.17387423G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387423G>C , CM000673.2:g.17387423G>C	GRCh38
NC_000011.9:g.17408970G>C , CM000673.1:g.17408970G>C	GRCh37
NC_000011.8:g.17365546G>C	NCBI36
NG_012446.1:g.6237C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682350.1:c.408C>G	ENSP00000508090.1:p.Thr136=
ENST00000682764.1:c.408C>G	ENSP00000506780.1:p.Thr136=
ENST00000339994.5:c.669C>G MANE Select	ENSP00000345708.4:p.Thr223=
ENST00000339994.4:c.669C>G	ENSP00000345708.4:p.Thr223=
ENST00000526912.1:c.408C>G	ENSP00000432729.1:p.Thr136=
ENST00000528731.1:c.408C>G	ENSP00000434755.1:p.Thr136=
NM_000525.3:c.669C>G	NP_000516.3:p.Thr223=
NM_001166290.1:c.408C>G	NP_001159762.1:p.Thr136=
XM_006718226.2:c.408C>G	XP_006718289.1:p.Thr136=
XR_930867.1:n.827C>G
XM_006718226.3:c.408C>G	XP_006718289.1:p.Thr136=
XM_017017680.1:c.408C>G	XP_016873169.1:p.Thr136=
NM_001166290.2:c.408C>G	NP_001159762.1:p.Thr136=
NM_001377296.1:c.408C>G	NP_001364225.1:p.Thr136=
NM_001377297.1:c.408C>G	NP_001364226.1:p.Thr136=
NM_000525.4:c.669C>G MANE Select	NP_000516.3:p.Thr223=