Canonical Allele Identifier: CA439137948
Gene: KLB HGNC NCBI

Linked Data

gnomAD v4: 4-39446934-G-A
MyVariant Identifiers: chr4:g.39448554G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446934G>A , CM000666.2:g.39446934G>A GRCh38
NC_000004.11:g.39448554G>A , CM000666.1:g.39448554G>A GRCh37
NC_000004.10:g.39124949G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2208G>A MANE Select ENSP00000257408.4:p.Gly736=
ENST00000257408.4:c.2208G>A ENSP00000257408.4:p.Gly736=
NM_175737.3:c.2208G>A NP_783864.1:p.Gly736=
XM_005262644.1:c.2181G>A XP_005262701.1:p.Gly727=
NM_175737.4:c.2208G>A MANE Select NP_783864.1:p.Gly736=
Search 100 bp 5'
Search 100 bp 3'