Canonical Allele Identifier: CA501202399

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914917G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837557G>T , CM000679.2:g.63837557G>T	GRCh38
NC_000017.10:g.61914917G>T , CM000679.1:g.61914917G>T	GRCh37
NC_000017.9:g.59268649G>T	NCBI36
NG_053004.1:g.10435C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.173C>A
ENST00000698016.1:c.144C>A	ENSP00000513502.1:p.Ser48=
ENST00000698022.1:c.102C>A	ENSP00000513504.1:p.Ser34=
ENST00000698027.1:c.144C>A	ENSP00000513505.1:p.Ser48=
ENST00000448276.7:c.285C>A MANE Select	ENSP00000392617.2:p.Ser95=
ENST00000225742.13:c.60C>A	ENSP00000225742.9:p.Ser20=
ENST00000323347.14:c.141C>A	ENSP00000318451.10:p.Ser47=
ENST00000448276.6:c.285C>A	ENSP00000392617.2:p.Ser95=
ENST00000577686.1:n.53-320C>A
ENST00000580054.1:c.69C>A	ENSP00000463793.1:p.Ser23=
ENST00000584400.5:c.217-320C>A	ENSP00000464503.1:n.217-320C>A
ENST00000613943.4:c.174C>A	ENSP00000483605.1:p.Ser58=
NM_001098426.1:c.285C>A	NP_001091896.1:p.Ser95=
XM_005257604.2:c.60C>A	XP_005257661.2:p.Ser20=
NM_001330439.1:c.60C>A	NP_001317368.1:p.Ser20=
NM_001330440.1:c.141C>A	NP_001317369.1:p.Ser47=
NM_001098426.2:c.285C>A MANE Select	NP_001091896.1:p.Ser95=
NM_001330440.2:c.141C>A	NP_001317369.1:p.Ser47=