Canonical Allele Identifier: CA507093784

Gene: TYROBP

Linked Data

• MyVariant Identifiers: chr19:g.36398463C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907561C>G , CM000681.2:g.35907561C>G	GRCh38
NC_000019.9:g.36398463C>G , CM000681.1:g.36398463C>G	GRCh37
NC_000019.8:g.41090303C>G	NCBI36
NG_009304.1:g.5724G>C , LRG_607:g.5724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.114G>C MANE Select	ENSP00000262629.3:p.Val38=
ENST00000262629.8:c.114G>C	ENSP00000262629.3:p.Val38=
ENST00000424586.7:c.81G>C	ENSP00000402371.3:p.Val27=
ENST00000544690.6:c.81G>C	ENSP00000445332.1:p.Val27=
ENST00000585626.1:n.181G>C
ENST00000585901.6:c.114G>C	ENSP00000468608.1:p.Val38=
ENST00000586946.1:c.107G>C	ENSP00000465656.1:p.Ter36Ser
ENST00000587837.5:c.107G>C	ENSP00000465081.1:p.Ter36Ser
ENST00000588439.1:n.258G>C
ENST00000589517.1:c.114G>C	ENSP00000468447.1:p.Val38=
NM_001173514.1:c.81G>C	NP_001166985.1:p.Val27=
NM_001173515.1:c.81G>C	NP_001166986.1:p.Val27=
NM_003332.3:c.114G>C , LRG_607t1:c.114G>C	NP_003323.1:p.Val38=
NM_198125.2:c.114G>C	NP_937758.1:p.Val38=
NR_033390.1:n.155G>C
NM_001173514.2:c.81G>C	NP_001166985.1:p.Val27=
NM_001173515.2:c.81G>C	NP_001166986.1:p.Val27=
NM_003332.4:c.114G>C MANE Select	NP_003323.1:p.Val38=
NM_198125.3:c.114G>C	NP_937758.1:p.Val38=
NR_033390.2:n.141G>C