Canonical Allele Identifier: CA490899125

Gene: KBTBD13

Linked Data

• MyVariant Identifiers: chr15:g.65369939C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65077601C>G , CM000677.2:g.65077601C>G	GRCh38
NC_000015.9:g.65369939C>G , CM000677.1:g.65369939C>G	GRCh37
NC_000015.8:g.63156992C>G	NCBI36
NG_021411.1:g.5786C>G , LRG_682:g.5786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432196.5:c.786C>G MANE Select	ENSP00000388723.2:p.Ala262=
ENST00000432196.3:c.786C>G	ENSP00000388723.2:p.Ala262=
NM_001101362.2:c.786C>G , LRG_682t1:c.786C>G	NP_001094832.1:p.Ala262=
NM_001101362.3:c.786C>G MANE Select	NP_001094832.1:p.Ala262=