Canonical Allele Identifier: CA253524
Gene: KCNE3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 5542
dbSNP Id: rs121908441

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74457268C>T , CM000673.2:g.74457268C>T GRCh38
NC_000011.9:g.74168313C>T , CM000673.1:g.74168313C>T GRCh37
NC_000011.8:g.73845961C>T NCBI36
NG_011833.1:g.15288G>A , LRG_439:g.15288G>A

Transcript Alleles

HGVS Amino-acid change
NM_005472.4:c.296G>A , LRG_439t1:c.296G>A NP_005463.1:p.Arg99His
XM_011544713.1:c.428G>A XP_011543015.1:p.Arg143His
XM_011544713.2:c.428G>A XP_011543015.1:p.Arg143His
XM_017017047.1:c.296G>A XP_016872536.1:p.Arg99His
XM_017017048.1:c.296G>A XP_016872537.1:p.Arg99His
XM_017017049.1:c.296G>A XP_016872538.1:p.Arg99His
XM_017017051.2:c.296G>A XP_016872540.1:p.Arg99His
XM_017017052.1:c.296G>A XP_016872541.1:p.Arg99His
ENST00000310128.8:c.296G>A ENSP00000310557.4:p.Arg99His
ENST00000525550.1:c.296G>A ENSP00000433633.1:p.Arg99His
ENST00000532569.5:c.296G>A ENSP00000431739.1:p.Arg99His