Canonical Allele Identifier: CA410196683

Gene: KCNE2

Linked Data

• COSMIC: COSM4101427
• MyVariant Identifiers: chr21:g.35742989C>G (hg19) ; chr21:g.34370690C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34370690C>G , CM000683.2:g.34370690C>G	GRCh38
NC_000021.8:g.35742989C>G , CM000683.1:g.35742989C>G	GRCh37
NC_000021.7:g.34664859C>G	NCBI36
NG_008804.1:g.11667C>G , LRG_291:g.11667C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290310.4:c.212C>G MANE Select	ENSP00000290310.2:p.Thr71Ser
ENST00000290310.3:c.212C>G	ENSP00000290310.2:p.Thr71Ser
NM_172201.1:c.212C>G , LRG_291t1:c.212C>G	NP_751951.1:p.Thr71Ser
XR_937683.1:n.631G>C
XR_937684.1:n.631G>C
XR_001755012.2:n.752G>C
XR_001755013.2:n.631G>C
XR_937683.2:n.631G>C
NM_172201.2:c.212C>G MANE Select	NP_751951.1:p.Thr71Ser