Canonical Allele Identifier: CA10013398
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs369159493

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370560C>T , CM000683.2:g.34370560C>T GRCh38
NC_000021.8:g.35742859C>T , CM000683.1:g.35742859C>T GRCh37
NC_000021.7:g.34664729C>T NCBI36
NG_008804.1:g.11537C>T , LRG_291:g.11537C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.82C>T MANE Select ENSP00000290310.2:p.Gln28Ter
ENST00000290310.3:c.82C>T ENSP00000290310.2:p.Gln28Ter
NM_172201.1:c.82C>T , LRG_291t1:c.82C>T NP_751951.1:p.Gln28Ter
NM_172201.2:c.82C>T MANE Select NP_751951.1:p.Gln28Ter