Canonical Allele Identifier: CA356657322
Gene: KLB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446819G>T , CM000666.2:g.39446819G>T GRCh38
NC_000004.11:g.39448439G>T , CM000666.1:g.39448439G>T GRCh37
NC_000004.10:g.39124834G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2093G>T MANE Select ENSP00000257408.4:p.Ser698Ile
ENST00000257408.4:c.2093G>T ENSP00000257408.4:p.Ser698Ile
NM_175737.3:c.2093G>T NP_783864.1:p.Ser698Ile
XM_005262644.1:c.2066G>T XP_005262701.1:p.Ser689Ile
NM_175737.4:c.2093G>T MANE Select NP_783864.1:p.Ser698Ile