Canonical Allele Identifier: CA490898959
Gene: KBTBD13 HGNC NCBI

Linked Data

dbSNP Id: rs184130258
gnomAD v2: 15-65370134-C-T
gnomAD v4: 15-65077796-C-T
MyVariant Identifiers: chr15:g.65370134C>T (hg19) chr15:g.65077796C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.981C>T MANE Select ENSP00000388723.2:p.Thr327=
ENST00000432196.3:c.981C>T ENSP00000388723.2:p.Thr327=
NM_001101362.2:c.981C>T , LRG_682t1:c.981C>T NP_001094832.1:p.Thr327=
NM_001101362.3:c.981C>T MANE Select NP_001094832.1:p.Thr327=
Search 100 bp 5'
Search 100 bp 3'