Canonical Allele Identifier: CA512345253
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35742900T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370601T>C , CM000683.2:g.34370601T>C GRCh38
NC_000021.8:g.35742900T>C , CM000683.1:g.35742900T>C GRCh37
NC_000021.7:g.34664770T>C NCBI36
NG_008804.1:g.11578T>C , LRG_291:g.11578T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.123T>C MANE Select ENSP00000290310.2:p.Val41=
ENST00000290310.3:c.123T>C ENSP00000290310.2:p.Val41=
NM_172201.1:c.123T>C , LRG_291t1:c.123T>C NP_751951.1:p.Val41=
XR_937683.1:n.720A>G
XR_937684.1:n.720A>G
XR_001755012.2:n.841A>G
XR_001755013.2:n.720A>G
XR_937683.2:n.720A>G
NM_172201.2:c.123T>C MANE Select NP_751951.1:p.Val41=