Canonical Allele Identifier: CA2639298406

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832501-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832501T>C , CM000679.2:g.63832501T>C	GRCh38
NC_000017.10:g.61909861T>C , CM000679.1:g.61909861T>C	GRCh37
NC_000017.9:g.59263593T>C	NCBI36
NG_053004.1:g.15491A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2312A>G
ENST00000697953.1:n.2885A>G
ENST00000698013.1:n.2997A>G
ENST00000698014.1:n.3220A>G
ENST00000698015.1:n.2313A>G
ENST00000698016.1:c.*437A>G	ENSP00000513502.1:n.*437A>G
ENST00000698017.1:n.2387A>G
ENST00000698018.1:n.2518A>G
ENST00000698019.1:n.2716A>G
ENST00000698020.1:n.1822A>G
ENST00000698021.1:c.1731A>G
ENST00000698022.1:c.*437A>G	ENSP00000513504.1:n.*437A>G
ENST00000698023.1:n.2416A>G
ENST00000698024.1:n.2278A>G
ENST00000698025.1:n.2438A>G
ENST00000698026.1:n.1329A>G
ENST00000698027.1:c.*654A>G	ENSP00000513505.1:n.*654A>G
ENST00000698028.1:n.2521A>G
ENST00000698029.1:n.3250A>G
ENST00000448276.7:c.*437A>G MANE Select	ENSP00000392617.2:n.*437A>G
ENST00000448276.6:c.*437A>G	ENSP00000392617.2:n.*437A>G
ENST00000613943.4:c.1922A>G	ENSP00000483605.1:n.1922A>G
NM_001098426.1:c.*437A>G	NP_001091896.1:n.*437A>G
XM_005257604.2:c.*437A>G	XP_005257661.2:n.*437A>G
NM_001330439.1:c.*437A>G	NP_001317368.1:n.*437A>G
NM_001330440.1:c.*437A>G	NP_001317369.1:n.*437A>G
NM_001098426.2:c.*437A>G MANE Select	NP_001091896.1:n.*437A>G
NM_001330440.2:c.*437A>G	NP_001317369.1:n.*437A>G