Canonical Allele Identifier: CA490898934
Gene: KBTBD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65369858C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077520C>G , CM000677.2:g.65077520C>G GRCh38
NC_000015.9:g.65369858C>G , CM000677.1:g.65369858C>G GRCh37
NC_000015.8:g.63156911C>G NCBI36
NG_021411.1:g.5705C>G , LRG_682:g.5705C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.705C>G MANE Select ENSP00000388723.2:p.Gly235=
ENST00000432196.3:c.705C>G ENSP00000388723.2:p.Gly235=
NM_001101362.2:c.705C>G , LRG_682t1:c.705C>G NP_001094832.1:p.Gly235=
NM_001101362.3:c.705C>G MANE Select NP_001094832.1:p.Gly235=