Canonical Allele Identifier: CA1452185052
Gene: KLB HGNC NCBI

Linked Data

dbSNP Id: rs1743324717

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430569T>C , CM000666.2:g.39430569T>C GRCh38
NC_000004.11:g.39432189T>C , CM000666.1:g.39432189T>C GRCh37
NC_000004.10:g.39108584T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.826-3641T>C MANE Select ENSP00000257408.4:n.826-3641T>C
ENST00000257408.4:c.826-3641T>C ENSP00000257408.4:n.826-3641T>C
NM_175737.3:c.826-3641T>C NP_783864.1:n.826-3641T>C
XM_005262644.1:c.826-3641T>C XP_005262701.1:n.826-3641T>C
NM_175737.4:c.826-3641T>C MANE Select NP_783864.1:n.826-3641T>C