Canonical Allele Identifier: CA734048495

Gene: SMYD3

Linked Data

• dbSNP Id: rs10802346
• MyVariant Identifiers: chr1:g.246372880G>A (hg19) ; chr1:g.246209578G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.246209578G>A , CM000663.2:g.246209578G>A	GRCh38
NC_000001.10:g.246372880G>A , CM000663.1:g.246372880G>A	GRCh37
NC_000001.9:g.244439503G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000490107.6:c.531+117623C>T MANE Select	ENSP00000419184.2:n.531+117623C>T
ENST00000453676.5:c.354+117623C>T	ENSP00000408122.1:n.354+117623C>T
ENST00000462422.5:n.458+117623C>T
ENST00000490107.5:c.531+117623C>T	ENSP00000419184.2:n.531+117623C>T
ENST00000492487.5:n.91+96341C>T
ENST00000630181.2:c.354+117623C>T	ENSP00000487434.1:n.354+117623C>T
NM_001167740.1:c.531+117623C>T	NP_001161212.1:n.531+117623C>T
NM_022743.2:c.354+117623C>T	NP_073580.1:n.354+117623C>T
XM_011544253.1:c.531+117623C>T	XP_011542555.1:n.531+117623C>T
XM_011544256.1:c.24+9868C>T	XP_011542558.1:n.24+9868C>T
XR_949153.1:n.632+117623C>T
XM_017002094.2:c.-37+73013C>T	XP_016857583.1:n.-37+73013C>T
XM_024449136.1:c.354+117623C>T	XP_024304904.1:n.354+117623C>T
XM_024449137.1:c.354+117623C>T	XP_024304905.1:n.354+117623C>T
XM_024449162.1:c.-37+10225C>T	XP_024304930.1:n.-37+10225C>T
NM_001167740.2:c.531+117623C>T MANE Select	NP_001161212.1:n.531+117623C>T
NM_001375962.1:c.531+117623C>T	NP_001362891.1:n.531+117623C>T
NM_001375963.1:c.354+117623C>T	NP_001362892.1:n.354+117623C>T
NM_022743.3:c.354+117623C>T	NP_073580.1:n.354+117623C>T