Canonical Allele Identifier: CA410196358

Gene: KCNE2

Linked Data

• dbSNP Id: rs1273269997
• MyVariant Identifiers: chr21:g.35742899T>G (hg19) ; chr21:g.34370600T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34370600T>G , CM000683.2:g.34370600T>G	GRCh38
NC_000021.8:g.35742899T>G , CM000683.1:g.35742899T>G	GRCh37
NC_000021.7:g.34664769T>G	NCBI36
NG_008804.1:g.11577T>G , LRG_291:g.11577T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290310.4:c.122T>G MANE Select	ENSP00000290310.2:p.Val41Gly
ENST00000290310.3:c.122T>G	ENSP00000290310.2:p.Val41Gly
NM_172201.1:c.122T>G , LRG_291t1:c.122T>G	NP_751951.1:p.Val41Gly
XR_937683.1:n.721A>C
XR_937684.1:n.721A>C
XR_001755012.2:n.842A>C
XR_001755013.2:n.721A>C
XR_937683.2:n.721A>C
NM_172201.2:c.122T>G MANE Select	NP_751951.1:p.Val41Gly