Canonical Allele Identifier: CA10013409
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs779623946
ExAC: 21:35742918 C / A
gnomAD v2: 21-35742918-C-A
gnomAD v3: 21-34370619-C-A
gnomAD v4: 21-34370619-C-A
MyVariant Identifiers: chr21:g.35742918C>A (hg19) chr21:g.34370619C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370619C>A , CM000683.2:g.34370619C>A GRCh38
NC_000021.8:g.35742918C>A , CM000683.1:g.35742918C>A GRCh37
NC_000021.7:g.34664788C>A NCBI36
NG_008804.1:g.11596C>A , LRG_291:g.11596C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.141C>A MANE Select ENSP00000290310.2:p.Tyr47Ter
ENST00000290310.3:c.141C>A ENSP00000290310.2:p.Tyr47Ter
NM_172201.1:c.141C>A , LRG_291t1:c.141C>A NP_751951.1:p.Tyr47Ter
XR_937683.1:n.702G>T
XR_937684.1:n.702G>T
XR_001755012.2:n.823G>T
XR_001755013.2:n.702G>T
XR_937683.2:n.702G>T
NM_172201.2:c.141C>A MANE Select NP_751951.1:p.Tyr47Ter
Search 100 bp 5'
Search 100 bp 3'