Canonical Allele Identifier: CA2270103094

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2040204254
• gnomAD v4: 17-63832474-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832474G>A , CM000679.2:g.63832474G>A	GRCh38
NC_000017.10:g.61909834G>A , CM000679.1:g.61909834G>A	GRCh37
NC_000017.9:g.59263566G>A	NCBI36
NG_053004.1:g.15518C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2339C>T
ENST00000697953.1:n.2912C>T
ENST00000698013.1:n.3024C>T
ENST00000698014.1:n.3247C>T
ENST00000698015.1:n.2340C>T
ENST00000698016.1:c.*464C>T	ENSP00000513502.1:n.*464C>T
ENST00000698017.1:n.2414C>T
ENST00000698018.1:n.2545C>T
ENST00000698019.1:n.2743C>T
ENST00000698020.1:n.1849C>T
ENST00000698021.1:c.1758C>T
ENST00000698022.1:c.*464C>T	ENSP00000513504.1:n.*464C>T
ENST00000698023.1:n.2443C>T
ENST00000698024.1:n.2305C>T
ENST00000698025.1:n.2465C>T
ENST00000698026.1:n.1356C>T
ENST00000698027.1:c.*681C>T	ENSP00000513505.1:n.*681C>T
ENST00000698028.1:n.2548C>T
ENST00000698029.1:n.3277C>T
ENST00000448276.7:c.*464C>T MANE Select	ENSP00000392617.2:n.*464C>T
ENST00000448276.6:c.*464C>T	ENSP00000392617.2:n.*464C>T
ENST00000613943.4:c.1949C>T	ENSP00000483605.1:n.1949C>T
NM_001098426.1:c.*464C>T	NP_001091896.1:n.*464C>T
XM_005257604.2:c.*464C>T	XP_005257661.2:n.*464C>T
NM_001330439.1:c.*464C>T	NP_001317368.1:n.*464C>T
NM_001330440.1:c.*464C>T	NP_001317369.1:n.*464C>T
NM_001098426.2:c.*464C>T MANE Select	NP_001091896.1:n.*464C>T
NM_001330440.2:c.*464C>T	NP_001317369.1:n.*464C>T