Canonical Allele Identifier: CA490898955
Gene: KBTBD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65370131G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077793G>A , CM000677.2:g.65077793G>A GRCh38
NC_000015.9:g.65370131G>A , CM000677.1:g.65370131G>A GRCh37
NC_000015.8:g.63157184G>A NCBI36
NG_021411.1:g.5978G>A , LRG_682:g.5978G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.978G>A MANE Select ENSP00000388723.2:p.Arg326=
ENST00000432196.3:c.978G>A ENSP00000388723.2:p.Arg326=
NM_001101362.2:c.978G>A , LRG_682t1:c.978G>A NP_001094832.1:p.Arg326=
NM_001101362.3:c.978G>A MANE Select NP_001094832.1:p.Arg326=
Search 100 bp 5'
Search 100 bp 3'