Canonical Allele Identifier: CA10013399
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs772975913

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370567C>A , CM000683.2:g.34370567C>A GRCh38
NC_000021.8:g.35742866C>A , CM000683.1:g.35742866C>A GRCh37
NC_000021.7:g.34664736C>A NCBI36
NG_008804.1:g.11544C>A , LRG_291:g.11544C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.89C>A MANE Select ENSP00000290310.2:p.Thr30Lys
ENST00000290310.3:c.89C>A ENSP00000290310.2:p.Thr30Lys
NM_172201.1:c.89C>A , LRG_291t1:c.89C>A NP_751951.1:p.Thr30Lys
XR_937683.1:n.754G>T
XR_937684.1:n.754G>T
XR_001755012.2:n.875G>T
XR_001755013.2:n.754G>T
XR_937683.2:n.754G>T
NM_172201.2:c.89C>A MANE Select NP_751951.1:p.Thr30Lys