Canonical Allele Identifier: CA16603268

Gene: TYROBP

Linked Data

• ClinVar Variation Id: 377100
• ClinVar RCV Id: RCV000434575
• dbSNP Id: rs1057520133
• MyVariant Identifiers: chr19:g.36398435T>C (hg19) ; chr19:g.35907533T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907533T>C , CM000681.2:g.35907533T>C	GRCh38
NC_000019.9:g.36398435T>C , CM000681.1:g.36398435T>C	GRCh37
NC_000019.8:g.41090275T>C	NCBI36
NG_009304.1:g.5752A>G , LRG_607:g.5752A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.142A>G MANE Select	ENSP00000262629.3:p.Met48Val
ENST00000262629.8:c.142A>G	ENSP00000262629.3:p.Met48Val
ENST00000424586.7:c.109A>G	ENSP00000402371.3:p.Met37Val
ENST00000544690.6:c.109A>G	ENSP00000445332.1:p.Met37Val
ENST00000585626.1:n.209A>G
ENST00000585901.6:c.142A>G	ENSP00000468608.1:p.Met48Val
ENST00000586946.1:c.*27A>G	ENSP00000465656.1:n.*27A>G
ENST00000587837.5:c.*27A>G	ENSP00000465081.1:n.*27A>G
ENST00000588439.1:n.286A>G
ENST00000589517.1:c.142A>G	ENSP00000468447.1:p.Met48Val
NM_001173514.1:c.109A>G	NP_001166985.1:p.Met37Val
NM_001173515.1:c.109A>G	NP_001166986.1:p.Met37Val
NM_003332.3:c.142A>G , LRG_607t1:c.142A>G	NP_003323.1:p.Met48Val
NM_198125.2:c.142A>G	NP_937758.1:p.Met48Val
NR_033390.1:n.183A>G
NM_001173514.2:c.109A>G	NP_001166985.1:p.Met37Val
NM_001173515.2:c.109A>G	NP_001166986.1:p.Met37Val
NM_003332.4:c.142A>G MANE Select	NP_003323.1:p.Met48Val
NM_198125.3:c.142A>G	NP_937758.1:p.Met48Val
NR_033390.2:n.169A>G