Canonical Allele Identifier: CA2639298046

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832157-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832157C>T , CM000679.2:g.63832157C>T	GRCh38
NC_000017.10:g.61909517C>T , CM000679.1:g.61909517C>T	GRCh37
NC_000017.9:g.59263249C>T	NCBI36
NG_053004.1:g.15835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2656G>A
ENST00000697953.1:n.3229G>A
ENST00000698013.1:n.3341G>A
ENST00000698014.1:n.3564G>A
ENST00000698015.1:n.2657G>A
ENST00000698016.1:c.*781G>A	ENSP00000513502.1:n.*781G>A
ENST00000698017.1:n.2731G>A
ENST00000698018.1:n.2862G>A
ENST00000698019.1:n.3060G>A
ENST00000698020.1:n.2166G>A
ENST00000698021.1:c.2075G>A
ENST00000698022.1:c.*781G>A	ENSP00000513504.1:n.*781G>A
ENST00000698023.1:n.2760G>A
ENST00000698024.1:n.2622G>A
ENST00000698025.1:n.2782G>A
ENST00000698026.1:n.1673G>A
ENST00000698027.1:c.*998G>A	ENSP00000513505.1:n.*998G>A
ENST00000448276.7:c.*781G>A MANE Select	ENSP00000392617.2:n.*781G>A
ENST00000448276.6:c.*781G>A	ENSP00000392617.2:n.*781G>A
ENST00000613943.4:c.2266G>A	ENSP00000483605.1:n.2266G>A
NM_001098426.1:c.*781G>A	NP_001091896.1:n.*781G>A
XM_005257604.2:c.*781G>A	XP_005257661.2:n.*781G>A
NM_001330439.1:c.*781G>A	NP_001317368.1:n.*781G>A
NM_001330440.1:c.*781G>A	NP_001317369.1:n.*781G>A
NM_001098426.2:c.*781G>A MANE Select	NP_001091896.1:n.*781G>A
NM_001330440.2:c.*781G>A	NP_001317369.1:n.*781G>A