Canonical Allele Identifier: CA2270103086

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2040204052

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832461T>A , CM000679.2:g.63832461T>A	GRCh38
NC_000017.10:g.61909821T>A , CM000679.1:g.61909821T>A	GRCh37
NC_000017.9:g.59263553T>A	NCBI36
NG_053004.1:g.15531A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2352A>T
ENST00000697953.1:n.2925A>T
ENST00000698013.1:n.3037A>T
ENST00000698014.1:n.3260A>T
ENST00000698015.1:n.2353A>T
ENST00000698016.1:c.*477A>T	ENSP00000513502.1:n.*477A>T
ENST00000698017.1:n.2427A>T
ENST00000698018.1:n.2558A>T
ENST00000698019.1:n.2756A>T
ENST00000698020.1:n.1862A>T
ENST00000698021.1:c.1771A>T
ENST00000698022.1:c.*477A>T	ENSP00000513504.1:n.*477A>T
ENST00000698023.1:n.2456A>T
ENST00000698024.1:n.2318A>T
ENST00000698025.1:n.2478A>T
ENST00000698026.1:n.1369A>T
ENST00000698027.1:c.*694A>T	ENSP00000513505.1:n.*694A>T
ENST00000698028.1:n.2561A>T
ENST00000698029.1:n.3290A>T
ENST00000448276.7:c.*477A>T MANE Select	ENSP00000392617.2:n.*477A>T
ENST00000448276.6:c.*477A>T	ENSP00000392617.2:n.*477A>T
ENST00000613943.4:c.1962A>T	ENSP00000483605.1:n.1962A>T
NM_001098426.1:c.*477A>T	NP_001091896.1:n.*477A>T
XM_005257604.2:c.*477A>T	XP_005257661.2:n.*477A>T
NM_001330439.1:c.*477A>T	NP_001317368.1:n.*477A>T
NM_001330440.1:c.*477A>T	NP_001317369.1:n.*477A>T
NM_001098426.2:c.*477A>T MANE Select	NP_001091896.1:n.*477A>T
NM_001330440.2:c.*477A>T	NP_001317369.1:n.*477A>T