Canonical Allele Identifier: CA490899128

Gene: KBTBD13

Linked Data

• MyVariant Identifiers: chr15:g.65369768C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65077430C>G , CM000677.2:g.65077430C>G	GRCh38
NC_000015.9:g.65369768C>G , CM000677.1:g.65369768C>G	GRCh37
NC_000015.8:g.63156821C>G	NCBI36
NG_021411.1:g.5615C>G , LRG_682:g.5615C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432196.5:c.615C>G MANE Select	ENSP00000388723.2:p.Ala205=
ENST00000432196.3:c.615C>G	ENSP00000388723.2:p.Ala205=
NM_001101362.2:c.615C>G , LRG_682t1:c.615C>G	NP_001094832.1:p.Ala205=
NM_001101362.3:c.615C>G MANE Select	NP_001094832.1:p.Ala205=