Canonical Allele Identifier: CA490898965
Gene: KBTBD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 767347
ClinVar RCV Id: RCV000946063
dbSNP Id: rs1477394894
gnomAD v2: 15-65370137-C-T
gnomAD v3: 15-65077799-C-T
gnomAD v4: 15-65077799-C-T
MyVariant Identifiers: chr15:g.65370137C>T (hg19) chr15:g.65077799C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077799C>T , CM000677.2:g.65077799C>T GRCh38
NC_000015.9:g.65370137C>T , CM000677.1:g.65370137C>T GRCh37
NC_000015.8:g.63157190C>T NCBI36
NG_021411.1:g.5984C>T , LRG_682:g.5984C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.984C>T MANE Select ENSP00000388723.2:p.Asp328=
ENST00000432196.3:c.984C>T ENSP00000388723.2:p.Asp328=
NM_001101362.2:c.984C>T , LRG_682t1:c.984C>T NP_001094832.1:p.Asp328=
NM_001101362.3:c.984C>T MANE Select NP_001094832.1:p.Asp328=
Search 100 bp 5'
Search 100 bp 3'