Canonical Allele Identifier: CA473515425
Gene: KCNJ11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17408862A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387315A>G , CM000673.2:g.17387315A>G GRCh38
NC_000011.9:g.17408862A>G , CM000673.1:g.17408862A>G GRCh37
NC_000011.8:g.17365438A>G NCBI36
NG_012446.1:g.6345T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.516T>C ENSP00000508090.1:p.His172=
ENST00000682764.1:c.516T>C ENSP00000506780.1:p.His172=
ENST00000339994.5:c.777T>C MANE Select ENSP00000345708.4:p.His259=
ENST00000339994.4:c.777T>C ENSP00000345708.4:p.His259=
ENST00000528731.1:c.516T>C ENSP00000434755.1:p.His172=
NM_000525.3:c.777T>C NP_000516.3:p.His259=
NM_001166290.1:c.516T>C NP_001159762.1:p.His172=
XM_006718226.2:c.516T>C XP_006718289.1:p.His172=
XR_930867.1:n.935T>C
XM_006718226.3:c.516T>C XP_006718289.1:p.His172=
XM_017017680.1:c.516T>C XP_016873169.1:p.His172=
NM_001166290.2:c.516T>C NP_001159762.1:p.His172=
NM_001377296.1:c.516T>C NP_001364225.1:p.His172=
NM_001377297.1:c.516T>C NP_001364226.1:p.His172=
NM_000525.4:c.777T>C MANE Select NP_000516.3:p.His259=