Canonical Allele Identifier: CA392862496
Gene: KBTBD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 567176
ClinVar RCV Id: RCV000687183
dbSNP Id: rs761192296
gnomAD v2: 15-65369855-C-G
gnomAD v4: 15-65077517-C-G
MyVariant Identifiers: chr15:g.65369855C>G (hg19) chr15:g.65077517C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077517C>G , CM000677.2:g.65077517C>G GRCh38
NC_000015.9:g.65369855C>G , CM000677.1:g.65369855C>G GRCh37
NC_000015.8:g.63156908C>G NCBI36
NG_021411.1:g.5702C>G , LRG_682:g.5702C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.702C>G MANE Select ENSP00000388723.2:p.Asp234Glu
ENST00000432196.3:c.702C>G ENSP00000388723.2:p.Asp234Glu
NM_001101362.2:c.702C>G , LRG_682t1:c.702C>G NP_001094832.1:p.Asp234Glu
NM_001101362.3:c.702C>G MANE Select NP_001094832.1:p.Asp234Glu
Search 100 bp 5'
Search 100 bp 3'