Canonical Allele Identifier: CA501202357

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914884G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837524G>A , CM000679.2:g.63837524G>A	GRCh38
NC_000017.10:g.61914884G>A , CM000679.1:g.61914884G>A	GRCh37
NC_000017.9:g.59268616G>A	NCBI36
NG_053004.1:g.10468C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.206C>T
ENST00000698016.1:c.177C>T	ENSP00000513502.1:p.Gly59=
ENST00000698022.1:c.135C>T	ENSP00000513504.1:p.Gly45=
ENST00000698027.1:c.177C>T	ENSP00000513505.1:p.Gly59=
ENST00000448276.7:c.318C>T MANE Select	ENSP00000392617.2:p.Gly106=
ENST00000225742.13:c.93C>T	ENSP00000225742.9:p.Gly31=
ENST00000323347.14:c.174C>T	ENSP00000318451.10:p.Gly58=
ENST00000448276.6:c.318C>T	ENSP00000392617.2:p.Gly106=
ENST00000577686.1:n.53-287C>T
ENST00000580054.1:c.102C>T	ENSP00000463793.1:p.Gly34=
ENST00000584400.5:c.217-287C>T	ENSP00000464503.1:n.217-287C>T
ENST00000613943.4:c.207C>T	ENSP00000483605.1:p.Gly69=
NM_001098426.1:c.318C>T	NP_001091896.1:p.Gly106=
XM_005257604.2:c.93C>T	XP_005257661.2:p.Gly31=
NM_001330439.1:c.93C>T	NP_001317368.1:p.Gly31=
NM_001330440.1:c.174C>T	NP_001317369.1:p.Gly58=
NM_001098426.2:c.318C>T MANE Select	NP_001091896.1:p.Gly106=
NM_001330440.2:c.174C>T	NP_001317369.1:p.Gly58=