Canonical Allele Identifier: CA512345069
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35742837T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370538T>A , CM000683.2:g.34370538T>A GRCh38
NC_000021.8:g.35742837T>A , CM000683.1:g.35742837T>A GRCh37
NC_000021.7:g.34664707T>A NCBI36
NG_008804.1:g.11515T>A , LRG_291:g.11515T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.60T>A MANE Select ENSP00000290310.2:p.Ile20=
ENST00000290310.3:c.60T>A ENSP00000290310.2:p.Ile20=
NM_172201.1:c.60T>A , LRG_291t1:c.60T>A NP_751951.1:p.Ile20=
XR_937683.1:n.783A>T
XR_937684.1:n.783A>T
XR_001755012.2:n.904A>T
XR_001755013.2:n.783A>T
XR_937683.2:n.783A>T
NM_172201.2:c.60T>A MANE Select NP_751951.1:p.Ile20=