Canonical Allele Identifier: CA2639298032

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832148-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832148C>A , CM000679.2:g.63832148C>A	GRCh38
NC_000017.10:g.61909508C>A , CM000679.1:g.61909508C>A	GRCh37
NC_000017.9:g.59263240C>A	NCBI36
NG_053004.1:g.15844G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2665G>T
ENST00000697953.1:n.3238G>T
ENST00000698013.1:n.3350G>T
ENST00000698014.1:n.3573G>T
ENST00000698015.1:n.2666G>T
ENST00000698016.1:c.*790G>T	ENSP00000513502.1:n.*790G>T
ENST00000698017.1:n.2740G>T
ENST00000698018.1:n.2871G>T
ENST00000698019.1:n.3069G>T
ENST00000698020.1:n.2175G>T
ENST00000698021.1:c.2084G>T
ENST00000698022.1:c.*790G>T	ENSP00000513504.1:n.*790G>T
ENST00000698023.1:n.2769G>T
ENST00000698024.1:n.2631G>T
ENST00000698025.1:n.2791G>T
ENST00000698026.1:n.1682G>T
ENST00000698027.1:c.*1007G>T	ENSP00000513505.1:n.*1007G>T
ENST00000448276.7:c.*790G>T MANE Select	ENSP00000392617.2:n.*790G>T
ENST00000448276.6:c.*790G>T	ENSP00000392617.2:n.*790G>T
ENST00000613943.4:c.2275G>T	ENSP00000483605.1:n.2275G>T
NM_001098426.1:c.*790G>T	NP_001091896.1:n.*790G>T
XM_005257604.2:c.*790G>T	XP_005257661.2:n.*790G>T
NM_001330439.1:c.*790G>T	NP_001317368.1:n.*790G>T
NM_001330440.1:c.*790G>T	NP_001317369.1:n.*790G>T
NM_001098426.2:c.*790G>T MANE Select	NP_001091896.1:n.*790G>T
NM_001330440.2:c.*790G>T	NP_001317369.1:n.*790G>T