Canonical Allele Identifier: CA835250557

Gene: SMARCD3

Linked Data

• dbSNP Id: rs1180966086
• gnomAD v3: 7-151253778-C-T
• gnomAD v4: 7-151253778-C-T
• MyVariant Identifiers: chr7:g.150950864C>T (hg19) ; chr7:g.151253778C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151253778C>T , CM000669.2:g.151253778C>T	GRCh38
NC_000007.13:g.150950864C>T , CM000669.1:g.150950864C>T	GRCh37
NC_000007.12:g.150581797C>T	NCBI36
NG_029468.1:g.28368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356800.6:c.40-8107G>A	ENSP00000349254.2:n.40-8107G>A
ENST00000392811.6:c.40-8107G>A	ENSP00000376558.2:n.40-8107G>A
ENST00000469154.5:c.71-10077G>A	ENSP00000417908.1:n.71-10077G>A
ENST00000477169.5:n.184+517G>A
ENST00000491651.1:c.40-8107G>A	ENSP00000419886.1:n.40-8107G>A
NM_001003802.1:c.40-8107G>A	NP_001003802.1:n.40-8107G>A
NM_003078.3:c.40-8107G>A	NP_003069.2:n.40-8107G>A
XM_011516521.1:c.-16-10077G>A	XP_011514823.1:n.-16-10077G>A
XR_928174.1:n.717-535C>T
XM_011516521.2:c.-16-10077G>A	XP_011514823.1:n.-16-10077G>A
XM_024446887.1:c.40-8107G>A	XP_024302655.1:n.40-8107G>A
XM_024446888.1:c.-16-10077G>A	XP_024302656.1:n.-16-10077G>A
XM_024446889.1:c.-221-10077G>A	XP_024302657.1:n.-221-10077G>A
NM_003078.4:c.40-8107G>A	NP_003069.2:n.40-8107G>A
NM_001003802.2:c.40-8107G>A	NP_001003802.1:n.40-8107G>A