Canonical Allele Identifier: CA2270103195

Gene: SMARCD2

Linked Data

• dbSNP Id: rs928472680

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832232A>C , CM000679.2:g.63832232A>C	GRCh38
NC_000017.10:g.61909592A>C , CM000679.1:g.61909592A>C	GRCh37
NC_000017.9:g.59263324A>C	NCBI36
NG_053004.1:g.15760T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2581T>G
ENST00000697953.1:n.3154T>G
ENST00000698013.1:n.3266T>G
ENST00000698014.1:n.3489T>G
ENST00000698015.1:n.2582T>G
ENST00000698016.1:c.*706T>G	ENSP00000513502.1:n.*706T>G
ENST00000698017.1:n.2656T>G
ENST00000698018.1:n.2787T>G
ENST00000698019.1:n.2985T>G
ENST00000698020.1:n.2091T>G
ENST00000698021.1:c.2000T>G
ENST00000698022.1:c.*706T>G	ENSP00000513504.1:n.*706T>G
ENST00000698023.1:n.2685T>G
ENST00000698024.1:n.2547T>G
ENST00000698025.1:n.2707T>G
ENST00000698026.1:n.1598T>G
ENST00000698027.1:c.*923T>G	ENSP00000513505.1:n.*923T>G
ENST00000698028.1:n.2790T>G
ENST00000448276.7:c.*706T>G MANE Select	ENSP00000392617.2:n.*706T>G
ENST00000448276.6:c.*706T>G	ENSP00000392617.2:n.*706T>G
ENST00000613943.4:c.2191T>G	ENSP00000483605.1:n.2191T>G
NM_001098426.1:c.*706T>G	NP_001091896.1:n.*706T>G
XM_005257604.2:c.*706T>G	XP_005257661.2:n.*706T>G
NM_001330439.1:c.*706T>G	NP_001317368.1:n.*706T>G
NM_001330440.1:c.*706T>G	NP_001317369.1:n.*706T>G
NM_001098426.2:c.*706T>G MANE Select	NP_001091896.1:n.*706T>G
NM_001330440.2:c.*706T>G	NP_001317369.1:n.*706T>G