Canonical Allele Identifier: CA1452184997
Gene: KLB HGNC NCBI

Linked Data

dbSNP Id: rs1743324142

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430549A>T , CM000666.2:g.39430549A>T GRCh38
NC_000004.11:g.39432169A>T , CM000666.1:g.39432169A>T GRCh37
NC_000004.10:g.39108564A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000257408.5:c.826-3661A>T MANE Select ENSP00000257408.4:n.826-3661A>T
ENST00000257408.4:c.826-3661A>T ENSP00000257408.4:n.826-3661A>T
NM_175737.3:c.826-3661A>T NP_783864.1:n.826-3661A>T
XM_005262644.1:c.826-3661A>T XP_005262701.1:n.826-3661A>T
NM_175737.4:c.826-3661A>T MANE Select NP_783864.1:n.826-3661A>T