Canonical Allele Identifier: CA439138135
Gene: KLB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.39448428T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39446808T>C , CM000666.2:g.39446808T>C GRCh38
NC_000004.11:g.39448428T>C , CM000666.1:g.39448428T>C GRCh37
NC_000004.10:g.39124823T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.2082T>C MANE Select ENSP00000257408.4:p.Pro694=
ENST00000257408.4:c.2082T>C ENSP00000257408.4:p.Pro694=
NM_175737.3:c.2082T>C NP_783864.1:p.Pro694=
XM_005262644.1:c.2055T>C XP_005262701.1:p.Pro685=
NM_175737.4:c.2082T>C MANE Select NP_783864.1:p.Pro694=
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