Canonical Allele Identifier: CA490898962
Gene: KBTBD13 HGNC NCBI

Linked Data

dbSNP Id: rs1340243344

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077535G>A , CM000677.2:g.65077535G>A GRCh38
NC_000015.9:g.65369873G>A , CM000677.1:g.65369873G>A GRCh37
NC_000015.8:g.63156926G>A NCBI36
NG_021411.1:g.5720G>A , LRG_682:g.5720G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.720G>A MANE Select ENSP00000388723.2:p.Glu240=
ENST00000432196.3:c.720G>A ENSP00000388723.2:p.Glu240=
NM_001101362.2:c.720G>A , LRG_682t1:c.720G>A NP_001094832.1:p.Glu240=
NM_001101362.3:c.720G>A MANE Select NP_001094832.1:p.Glu240=