Canonical Allele Identifier: CA392864852
Gene: KBTBD13 HGNC NCBI

Linked Data

dbSNP Id: rs2087000535
gnomAD v4: 15-65077801-C-T
MyVariant Identifiers: chr15:g.65370139C>T (hg19) chr15:g.65077801C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077801C>T , CM000677.2:g.65077801C>T GRCh38
NC_000015.9:g.65370139C>T , CM000677.1:g.65370139C>T GRCh37
NC_000015.8:g.63157192C>T NCBI36
NG_021411.1:g.5986C>T , LRG_682:g.5986C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.986C>T MANE Select ENSP00000388723.2:p.Ala329Val
ENST00000432196.3:c.986C>T ENSP00000388723.2:p.Ala329Val
NM_001101362.2:c.986C>T , LRG_682t1:c.986C>T NP_001094832.1:p.Ala329Val
NM_001101362.3:c.986C>T MANE Select NP_001094832.1:p.Ala329Val
Search 100 bp 5'
Search 100 bp 3'