Canonical Allele Identifier: CA501202394

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914914T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837554T>G , CM000679.2:g.63837554T>G	GRCh38
NC_000017.10:g.61914914T>G , CM000679.1:g.61914914T>G	GRCh37
NC_000017.9:g.59268646T>G	NCBI36
NG_053004.1:g.10438A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.176A>C
ENST00000698016.1:c.147A>C	ENSP00000513502.1:p.Pro49=
ENST00000698022.1:c.105A>C	ENSP00000513504.1:p.Pro35=
ENST00000698027.1:c.147A>C	ENSP00000513505.1:p.Pro49=
ENST00000448276.7:c.288A>C MANE Select	ENSP00000392617.2:p.Pro96=
ENST00000225742.13:c.63A>C	ENSP00000225742.9:p.Pro21=
ENST00000323347.14:c.144A>C	ENSP00000318451.10:p.Pro48=
ENST00000448276.6:c.288A>C	ENSP00000392617.2:p.Pro96=
ENST00000577686.1:n.53-317A>C
ENST00000580054.1:c.72A>C	ENSP00000463793.1:p.Pro24=
ENST00000584400.5:c.217-317A>C	ENSP00000464503.1:n.217-317A>C
ENST00000613943.4:c.177A>C	ENSP00000483605.1:p.Pro59=
NM_001098426.1:c.288A>C	NP_001091896.1:p.Pro96=
XM_005257604.2:c.63A>C	XP_005257661.2:p.Pro21=
NM_001330439.1:c.63A>C	NP_001317368.1:p.Pro21=
NM_001330440.1:c.144A>C	NP_001317369.1:p.Pro48=
NM_001098426.2:c.288A>C MANE Select	NP_001091896.1:p.Pro96=
NM_001330440.2:c.144A>C	NP_001317369.1:p.Pro48=