Canonical Allele Identifier: CA1452184982
Gene: KLB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430541C= , CM000666.2:g.39430541C= GRCh38
NC_000004.11:g.39432161C= , CM000666.1:g.39432161C= GRCh37
NC_000004.10:g.39108556C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.826-3669C= MANE Select ENSP00000257408.4:n.826-3669C=
ENST00000257408.4:c.826-3669C= ENSP00000257408.4:n.826-3669C=
NM_175737.3:c.826-3669C= NP_783864.1:n.826-3669C=
XM_005262644.1:c.826-3669C= XP_005262701.1:n.826-3669C=
NM_175737.4:c.826-3669C= MANE Select NP_783864.1:n.826-3669C=