Canonical Allele Identifier: CA490899101
Gene: KBTBD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65369756G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077418G>C , CM000677.2:g.65077418G>C GRCh38
NC_000015.9:g.65369756G>C , CM000677.1:g.65369756G>C GRCh37
NC_000015.8:g.63156809G>C NCBI36
NG_021411.1:g.5603G>C , LRG_682:g.5603G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.603G>C MANE Select ENSP00000388723.2:p.Leu201=
ENST00000432196.3:c.603G>C ENSP00000388723.2:p.Leu201=
NM_001101362.2:c.603G>C , LRG_682t1:c.603G>C NP_001094832.1:p.Leu201=
NM_001101362.3:c.603G>C MANE Select NP_001094832.1:p.Leu201=
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