Canonical Allele Identifier: CA292951812

Gene: SMARCD2

Linked Data

• dbSNP Id: rs896713392
• gnomAD v3: 17-63832463-C-T
• gnomAD v4: 17-63832463-C-T
• MyVariant Identifiers: chr17:g.61909823C>T (hg19) ; chr17:g.63832463C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832463C>T , CM000679.2:g.63832463C>T	GRCh38
NC_000017.10:g.61909823C>T , CM000679.1:g.61909823C>T	GRCh37
NC_000017.9:g.59263555C>T	NCBI36
NG_053004.1:g.15529G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2350G>A
ENST00000697953.1:n.2923G>A
ENST00000698013.1:n.3035G>A
ENST00000698014.1:n.3258G>A
ENST00000698015.1:n.2351G>A
ENST00000698016.1:c.*475G>A	ENSP00000513502.1:n.*475G>A
ENST00000698017.1:n.2425G>A
ENST00000698018.1:n.2556G>A
ENST00000698019.1:n.2754G>A
ENST00000698020.1:n.1860G>A
ENST00000698021.1:c.1769G>A
ENST00000698022.1:c.*475G>A	ENSP00000513504.1:n.*475G>A
ENST00000698023.1:n.2454G>A
ENST00000698024.1:n.2316G>A
ENST00000698025.1:n.2476G>A
ENST00000698026.1:n.1367G>A
ENST00000698027.1:c.*692G>A	ENSP00000513505.1:n.*692G>A
ENST00000698028.1:n.2559G>A
ENST00000698029.1:n.3288G>A
ENST00000448276.7:c.*475G>A MANE Select	ENSP00000392617.2:n.*475G>A
ENST00000448276.6:c.*475G>A	ENSP00000392617.2:n.*475G>A
ENST00000613943.4:c.1960G>A	ENSP00000483605.1:n.1960G>A
NM_001098426.1:c.*475G>A	NP_001091896.1:n.*475G>A
XM_005257604.2:c.*475G>A	XP_005257661.2:n.*475G>A
NM_001330439.1:c.*475G>A	NP_001317368.1:n.*475G>A
NM_001330440.1:c.*475G>A	NP_001317369.1:n.*475G>A
NM_001098426.2:c.*475G>A MANE Select	NP_001091896.1:n.*475G>A
NM_001330440.2:c.*475G>A	NP_001317369.1:n.*475G>A