Canonical Allele Identifier: CA512345329
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35742951A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370652A>G , CM000683.2:g.34370652A>G GRCh38
NC_000021.8:g.35742951A>G , CM000683.1:g.35742951A>G GRCh37
NC_000021.7:g.34664821A>G NCBI36
NG_008804.1:g.11629A>G , LRG_291:g.11629A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.174A>G MANE Select ENSP00000290310.2:p.Gly58=
ENST00000290310.3:c.174A>G ENSP00000290310.2:p.Gly58=
NM_172201.1:c.174A>G , LRG_291t1:c.174A>G NP_751951.1:p.Gly58=
NM_172201.2:c.174A>G MANE Select NP_751951.1:p.Gly58=