Canonical Allele Identifier: CA7613985
Gene: KBTBD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1599028
ClinVar RCV Id: RCV002122978 RCV003951096
dbSNP Id: rs577503698
ExAC: 15:65369948 C / T
gnomAD v2: 15-65369948-C-T
gnomAD v3: 15-65077610-C-T
gnomAD v4: 15-65077610-C-T
MyVariant Identifiers: chr15:g.65369948C>T (hg19) chr15:g.65077610C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077610C>T , CM000677.2:g.65077610C>T GRCh38
NC_000015.9:g.65369948C>T , CM000677.1:g.65369948C>T GRCh37
NC_000015.8:g.63157001C>T NCBI36
NG_021411.1:g.5795C>T , LRG_682:g.5795C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.795C>T MANE Select ENSP00000388723.2:p.Gly265=
ENST00000432196.3:c.795C>T ENSP00000388723.2:p.Gly265=
NM_001101362.2:c.795C>T , LRG_682t1:c.795C>T NP_001094832.1:p.Gly265=
NM_001101362.3:c.795C>T MANE Select NP_001094832.1:p.Gly265=
Search 100 bp 5'
Search 100 bp 3'