Canonical Allele Identifier: CA439138153
Gene: KLB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.39448435C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446815C>T , CM000666.2:g.39446815C>T GRCh38
NC_000004.11:g.39448435C>T , CM000666.1:g.39448435C>T GRCh37
NC_000004.10:g.39124830C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2089C>T MANE Select ENSP00000257408.4:p.Leu697=
ENST00000257408.4:c.2089C>T ENSP00000257408.4:p.Leu697=
NM_175737.3:c.2089C>T NP_783864.1:p.Leu697=
XM_005262644.1:c.2062C>T XP_005262701.1:p.Leu688=
NM_175737.4:c.2089C>T MANE Select NP_783864.1:p.Leu697=
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