Canonical Allele Identifier: CA490899188
Gene: KBTBD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65369969C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077631C>T , CM000677.2:g.65077631C>T GRCh38
NC_000015.9:g.65369969C>T , CM000677.1:g.65369969C>T GRCh37
NC_000015.8:g.63157022C>T NCBI36
NG_021411.1:g.5816C>T , LRG_682:g.5816C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.816C>T MANE Select ENSP00000388723.2:p.Ile272=
ENST00000432196.3:c.816C>T ENSP00000388723.2:p.Ile272=
NM_001101362.2:c.816C>T , LRG_682t1:c.816C>T NP_001094832.1:p.Ile272=
NM_001101362.3:c.816C>T MANE Select NP_001094832.1:p.Ile272=