Canonical Allele Identifier: CA2639298389

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832479-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832479A>C , CM000679.2:g.63832479A>C	GRCh38
NC_000017.10:g.61909839A>C , CM000679.1:g.61909839A>C	GRCh37
NC_000017.9:g.59263571A>C	NCBI36
NG_053004.1:g.15513T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2334T>G
ENST00000697953.1:n.2907T>G
ENST00000698013.1:n.3019T>G
ENST00000698014.1:n.3242T>G
ENST00000698015.1:n.2335T>G
ENST00000698016.1:c.*459T>G	ENSP00000513502.1:n.*459T>G
ENST00000698017.1:n.2409T>G
ENST00000698018.1:n.2540T>G
ENST00000698019.1:n.2738T>G
ENST00000698020.1:n.1844T>G
ENST00000698021.1:c.1753T>G
ENST00000698022.1:c.*459T>G	ENSP00000513504.1:n.*459T>G
ENST00000698023.1:n.2438T>G
ENST00000698024.1:n.2300T>G
ENST00000698025.1:n.2460T>G
ENST00000698026.1:n.1351T>G
ENST00000698027.1:c.*676T>G	ENSP00000513505.1:n.*676T>G
ENST00000698028.1:n.2543T>G
ENST00000698029.1:n.3272T>G
ENST00000448276.7:c.*459T>G MANE Select	ENSP00000392617.2:n.*459T>G
ENST00000448276.6:c.*459T>G	ENSP00000392617.2:n.*459T>G
ENST00000613943.4:c.1944T>G	ENSP00000483605.1:n.1944T>G
NM_001098426.1:c.*459T>G	NP_001091896.1:n.*459T>G
XM_005257604.2:c.*459T>G	XP_005257661.2:n.*459T>G
NM_001330439.1:c.*459T>G	NP_001317368.1:n.*459T>G
NM_001330440.1:c.*459T>G	NP_001317369.1:n.*459T>G
NM_001098426.2:c.*459T>G MANE Select	NP_001091896.1:n.*459T>G
NM_001330440.2:c.*459T>G	NP_001317369.1:n.*459T>G