Canonical Allele Identifier: CA1452131107
Gene: KLB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446933G= , CM000666.2:g.39446933G= GRCh38
NC_000004.11:g.39448553G= , CM000666.1:g.39448553G= GRCh37
NC_000004.10:g.39124948G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2207G= MANE Select ENSP00000257408.4:p.Gly736=
ENST00000257408.4:c.2207G= ENSP00000257408.4:p.Gly736=
NM_175737.3:c.2207G= NP_783864.1:p.Gly736=
XM_005262644.1:c.2180G= XP_005262701.1:p.Gly727=
NM_175737.4:c.2207G= MANE Select NP_783864.1:p.Gly736=
Search 100 bp 5'
Search 100 bp 3'