Canonical Allele Identifier: CA1452185013
Gene: KLB HGNC NCBI

Linked Data

dbSNP Id: rs1743324242
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430560G>A , CM000666.2:g.39430560G>A GRCh38
NC_000004.11:g.39432180G>A , CM000666.1:g.39432180G>A GRCh37
NC_000004.10:g.39108575G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000257408.5:c.826-3650G>A MANE Select ENSP00000257408.4:n.826-3650G>A
ENST00000257408.4:c.826-3650G>A ENSP00000257408.4:n.826-3650G>A
NM_175737.3:c.826-3650G>A NP_783864.1:n.826-3650G>A
XM_005262644.1:c.826-3650G>A XP_005262701.1:n.826-3650G>A
NM_175737.4:c.826-3650G>A MANE Select NP_783864.1:n.826-3650G>A
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