Canonical Allele Identifier: CA501202306

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914833C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837473C>T , CM000679.2:g.63837473C>T	GRCh38
NC_000017.10:g.61914833C>T , CM000679.1:g.61914833C>T	GRCh37
NC_000017.9:g.59268565C>T	NCBI36
NG_053004.1:g.10519G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.257G>A
ENST00000698015.1:n.3G>A
ENST00000698016.1:c.228G>A	ENSP00000513502.1:p.Gln76=
ENST00000698021.1:c.32G>A
ENST00000698022.1:c.186G>A	ENSP00000513504.1:p.Gln62=
ENST00000698027.1:c.228G>A	ENSP00000513505.1:p.Gln76=
ENST00000448276.7:c.369G>A MANE Select	ENSP00000392617.2:p.Gln123=
ENST00000225742.13:c.144G>A	ENSP00000225742.9:p.Gln48=
ENST00000323347.14:c.225G>A	ENSP00000318451.10:p.Gln75=
ENST00000448276.6:c.369G>A	ENSP00000392617.2:p.Gln123=
ENST00000577686.1:n.53-236G>A
ENST00000580054.1:c.153G>A	ENSP00000463793.1:p.Gln51=
ENST00000584400.5:c.217-236G>A	ENSP00000464503.1:n.217-236G>A
ENST00000613943.4:c.258G>A	ENSP00000483605.1:p.Gln86=
NM_001098426.1:c.369G>A	NP_001091896.1:p.Gln123=
XM_005257604.2:c.144G>A	XP_005257661.2:p.Gln48=
NM_001330439.1:c.144G>A	NP_001317368.1:p.Gln48=
NM_001330440.1:c.225G>A	NP_001317369.1:p.Gln75=
NM_001098426.2:c.369G>A MANE Select	NP_001091896.1:p.Gln123=
NM_001330440.2:c.225G>A	NP_001317369.1:p.Gln75=