Canonical Allele Identifier: CA356657153
Gene: KLB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446765A>C , CM000666.2:g.39446765A>C GRCh38
NC_000004.11:g.39448385A>C , CM000666.1:g.39448385A>C GRCh37
NC_000004.10:g.39124780A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2039A>C MANE Select ENSP00000257408.4:p.Glu680Ala
ENST00000257408.4:c.2039A>C ENSP00000257408.4:p.Glu680Ala
NM_175737.3:c.2039A>C NP_783864.1:p.Glu680Ala
XM_005262644.1:c.2012A>C XP_005262701.1:p.Glu671Ala
NM_175737.4:c.2039A>C MANE Select NP_783864.1:p.Glu680Ala