Canonical Allele Identifier: CA10013400
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs757208768

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370570C>G , CM000683.2:g.34370570C>G GRCh38
NC_000021.8:g.35742869C>G , CM000683.1:g.35742869C>G GRCh37
NC_000021.7:g.34664739C>G NCBI36
NG_008804.1:g.11547C>G , LRG_291:g.11547C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.92C>G MANE Select ENSP00000290310.2:p.Thr31Arg
ENST00000290310.3:c.92C>G ENSP00000290310.2:p.Thr31Arg
NM_172201.1:c.92C>G , LRG_291t1:c.92C>G NP_751951.1:p.Thr31Arg
XR_937683.1:n.751G>C
XR_937684.1:n.751G>C
XR_001755012.2:n.872G>C
XR_001755013.2:n.751G>C
XR_937683.2:n.751G>C
NM_172201.2:c.92C>G MANE Select NP_751951.1:p.Thr31Arg