Canonical Allele Identifier: CA1452184989
Gene: KLB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430544G= , CM000666.2:g.39430544G= GRCh38
NC_000004.11:g.39432164G= , CM000666.1:g.39432164G= GRCh37
NC_000004.10:g.39108559G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.826-3666G= MANE Select ENSP00000257408.4:n.826-3666G=
ENST00000257408.4:c.826-3666G= ENSP00000257408.4:n.826-3666G=
NM_175737.3:c.826-3666G= NP_783864.1:n.826-3666G=
XM_005262644.1:c.826-3666G= XP_005262701.1:n.826-3666G=
NM_175737.4:c.826-3666G= MANE Select NP_783864.1:n.826-3666G=