Canonical Allele Identifier: CA392863383
Gene: KBTBD13 HGNC NCBI

Linked Data

dbSNP Id: rs2919359
gnomAD v4: 15-65077613-A-C
MyVariant Identifiers: chr15:g.65369951A>C (hg19) chr15:g.65077613A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077613A>C , CM000677.2:g.65077613A>C GRCh38
NC_000015.9:g.65369951A>C , CM000677.1:g.65369951A>C GRCh37
NC_000015.8:g.63157004A>C NCBI36
NG_021411.1:g.5798A>C , LRG_682:g.5798A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.798A>C MANE Select ENSP00000388723.2:p.Glu266Asp
ENST00000432196.3:c.798A>C ENSP00000388723.2:p.Glu266Asp
NM_001101362.2:c.798A>C , LRG_682t1:c.798A>C NP_001094832.1:p.Glu266Asp
NM_001101362.3:c.798A>C MANE Select NP_001094832.1:p.Glu266Asp
Search 100 bp 5'
Search 100 bp 3'