Canonical Allele Identifier: CA1452184974
Gene: KLB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430536A= , CM000666.2:g.39430536A= GRCh38
NC_000004.11:g.39432156A= , CM000666.1:g.39432156A= GRCh37
NC_000004.10:g.39108551A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000257408.5:c.826-3674A= MANE Select ENSP00000257408.4:n.826-3674A=
ENST00000257408.4:c.826-3674A= ENSP00000257408.4:n.826-3674A=
NM_175737.3:c.826-3674A= NP_783864.1:n.826-3674A=
XM_005262644.1:c.826-3674A= XP_005262701.1:n.826-3674A=
NM_175737.4:c.826-3674A= MANE Select NP_783864.1:n.826-3674A=
Search 100 bp 5'
Search 100 bp 3'