Canonical Allele Identifier: CA773992979

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1358112737
• gnomAD v3: 17-63832179-C-T
• gnomAD v4: 17-63832179-C-T
• MyVariant Identifiers: chr17:g.61909539C>T (hg19) ; chr17:g.63832179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832179C>T , CM000679.2:g.63832179C>T	GRCh38
NC_000017.10:g.61909539C>T , CM000679.1:g.61909539C>T	GRCh37
NC_000017.9:g.59263271C>T	NCBI36
NG_053004.1:g.15813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2634G>A
ENST00000697953.1:n.3207G>A
ENST00000698013.1:n.3319G>A
ENST00000698014.1:n.3542G>A
ENST00000698015.1:n.2635G>A
ENST00000698016.1:c.*759G>A	ENSP00000513502.1:n.*759G>A
ENST00000698017.1:n.2709G>A
ENST00000698018.1:n.2840G>A
ENST00000698019.1:n.3038G>A
ENST00000698020.1:n.2144G>A
ENST00000698021.1:c.2053G>A
ENST00000698022.1:c.*759G>A	ENSP00000513504.1:n.*759G>A
ENST00000698023.1:n.2738G>A
ENST00000698024.1:n.2600G>A
ENST00000698025.1:n.2760G>A
ENST00000698026.1:n.1651G>A
ENST00000698027.1:c.*976G>A	ENSP00000513505.1:n.*976G>A
ENST00000448276.7:c.*759G>A MANE Select	ENSP00000392617.2:n.*759G>A
ENST00000448276.6:c.*759G>A	ENSP00000392617.2:n.*759G>A
ENST00000613943.4:c.2244G>A	ENSP00000483605.1:n.2244G>A
NM_001098426.1:c.*759G>A	NP_001091896.1:n.*759G>A
XM_005257604.2:c.*759G>A	XP_005257661.2:n.*759G>A
NM_001330439.1:c.*759G>A	NP_001317368.1:n.*759G>A
NM_001330440.1:c.*759G>A	NP_001317369.1:n.*759G>A
NM_001098426.2:c.*759G>A MANE Select	NP_001091896.1:n.*759G>A
NM_001330440.2:c.*759G>A	NP_001317369.1:n.*759G>A