Canonical Allele Identifier: CA1452131100

Gene: KLB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39446922C= , CM000666.2:g.39446922C=	GRCh38
NC_000004.11:g.39448542C= , CM000666.1:g.39448542C=	GRCh37
NC_000004.10:g.39124937C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257408.5:c.2196C= MANE Select	ENSP00000257408.4:p.Pro732=
ENST00000257408.4:c.2196C=	ENSP00000257408.4:p.Pro732=
NM_175737.3:c.2196C=	NP_783864.1:p.Pro732=
XM_005262644.1:c.2169C=	XP_005262701.1:p.Pro723=
NM_175737.4:c.2196C= MANE Select	NP_783864.1:p.Pro732=