Canonical Allele Identifier: CA9393148

Gene: TYROBP

Linked Data

• dbSNP Id: rs184784706
• ExAC: 19:36399039 C / A
• gnomAD v2: 19-36399039-C-A
• gnomAD v3: 19-35908137-C-A
• gnomAD v4: 19-35908137-C-A
• MyVariant Identifiers: chr19:g.36399039C>A (hg19) ; chr19:g.36399039_36399040delinsAG (hg19) ; chr19:g.35908137C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35908137C>A , CM000681.2:g.35908137C>A	GRCh38
NC_000019.9:g.36399039C>A , CM000681.1:g.36399039C>A	GRCh37
NC_000019.8:g.41090879C>A	NCBI36
NG_009304.1:g.5148G>T , LRG_607:g.5148G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262629.9:c.61+31G>T MANE Select	ENSP00000262629.3:n.61+31G>T
ENST00000262629.8:c.61+31G>T	ENSP00000262629.3:n.61+31G>T
ENST00000424586.7:c.61+31G>T	ENSP00000402371.3:n.61+31G>T
ENST00000544690.6:c.61+31G>T	ENSP00000445332.1:n.61+31G>T
ENST00000585626.1:n.128+31G>T
ENST00000585901.6:c.61+31G>T	ENSP00000468608.1:n.61+31G>T
ENST00000586946.1:c.54+38G>T	ENSP00000465656.1:n.54+38G>T
ENST00000587837.5:c.54+38G>T	ENSP00000465081.1:n.54+38G>T
ENST00000588439.1:n.56+31G>T
ENST00000589517.1:c.61+31G>T	ENSP00000468447.1:n.61+31G>T
NM_001173514.1:c.61+31G>T	NP_001166985.1:n.61+31G>T
NM_001173515.1:c.61+31G>T	NP_001166986.1:n.61+31G>T
NM_003332.3:c.61+31G>T , LRG_607t1:c.61+31G>T	NP_003323.1:n.61+31G>T
NM_198125.2:c.61+31G>T	NP_937758.1:n.61+31G>T
NR_033390.1:n.135+38G>T
NM_001173514.2:c.61+31G>T	NP_001166985.1:n.61+31G>T
NM_001173515.2:c.61+31G>T	NP_001166986.1:n.61+31G>T
NM_003332.4:c.61+31G>T MANE Select	NP_003323.1:n.61+31G>T
NM_198125.3:c.61+31G>T	NP_937758.1:n.61+31G>T
NR_033390.2:n.121+38G>T