Canonical Allele Identifier: CA410196257
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs1307670975

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370566A>C , CM000683.2:g.34370566A>C GRCh38
NC_000021.8:g.35742865A>C , CM000683.1:g.35742865A>C GRCh37
NC_000021.7:g.34664735A>C NCBI36
NG_008804.1:g.11543A>C , LRG_291:g.11543A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.88A>C MANE Select ENSP00000290310.2:p.Thr30Pro
ENST00000290310.3:c.88A>C ENSP00000290310.2:p.Thr30Pro
NM_172201.1:c.88A>C , LRG_291t1:c.88A>C NP_751951.1:p.Thr30Pro
XR_937683.1:n.755T>G
XR_937684.1:n.755T>G
XR_001755012.2:n.876T>G
XR_001755013.2:n.755T>G
XR_937683.2:n.755T>G
NM_172201.2:c.88A>C MANE Select NP_751951.1:p.Thr30Pro