Canonical Allele Identifier: CA10013384
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs763870305

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370465A>G , CM000683.2:g.34370465A>G GRCh38
NC_000021.8:g.35742764A>G , CM000683.1:g.35742764A>G GRCh37
NC_000021.7:g.34664634A>G NCBI36
NG_008804.1:g.11442A>G , LRG_291:g.11442A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.-12-2A>G MANE Select ENSP00000290310.2:n.-12-2A>G
ENST00000290310.3:c.-12-2A>G ENSP00000290310.2:n.-12-2A>G
NM_172201.1:c.-12-2A>G , LRG_291t1:c.-12-2A>G NP_751951.1:n.-12-2A>G
XR_937683.1:n.856T>C
XR_937684.1:n.856T>C
XR_001755012.2:n.977T>C
XR_001755013.2:n.856T>C
XR_937683.2:n.856T>C
NM_172201.2:c.-12-2A>G MANE Select NP_751951.1:n.-12-2A>G