Canonical Allele Identifier: CA7614037
Gene: KBTBD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 316749
ClinVar RCV Id: RCV000540084 RCV001683274
dbSNP Id: rs184130258
ExAC: 15:65370134 C / G
gnomAD v2: 15-65370134-C-G
gnomAD v3: 15-65077796-C-G
gnomAD v4: 15-65077796-C-G
MyVariant Identifiers: chr15:g.65370134C>G (hg19) chr15:g.65077796C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077796C>G , CM000677.2:g.65077796C>G GRCh38
NC_000015.9:g.65370134C>G , CM000677.1:g.65370134C>G GRCh37
NC_000015.8:g.63157187C>G NCBI36
NG_021411.1:g.5981C>G , LRG_682:g.5981C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.981C>G MANE Select ENSP00000388723.2:p.Thr327=
ENST00000432196.3:c.981C>G ENSP00000388723.2:p.Thr327=
NM_001101362.2:c.981C>G , LRG_682t1:c.981C>G NP_001094832.1:p.Thr327=
NM_001101362.3:c.981C>G MANE Select NP_001094832.1:p.Thr327=
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