Canonical Allele Identifier: CA392863149
Gene: KBTBD13 HGNC NCBI

Linked Data

dbSNP Id: rs1360336920
gnomAD v2: 15-65369926-G-C
gnomAD v4: 15-65077588-G-C
MyVariant Identifiers: chr15:g.65369926G>C (hg19) chr15:g.65077588G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077588G>C , CM000677.2:g.65077588G>C GRCh38
NC_000015.9:g.65369926G>C , CM000677.1:g.65369926G>C GRCh37
NC_000015.8:g.63156979G>C NCBI36
NG_021411.1:g.5773G>C , LRG_682:g.5773G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.773G>C MANE Select ENSP00000388723.2:p.Gly258Ala
ENST00000432196.3:c.773G>C ENSP00000388723.2:p.Gly258Ala
NM_001101362.2:c.773G>C , LRG_682t1:c.773G>C NP_001094832.1:p.Gly258Ala
NM_001101362.3:c.773G>C MANE Select NP_001094832.1:p.Gly258Ala
Search 100 bp 5'
Search 100 bp 3'