Canonical Allele Identifier: CA578720409

Gene: SMARCD3

Linked Data

• dbSNP Id: rs1486764866
• gnomAD v2: 7-150950841-G-T
• gnomAD v3: 7-151253755-G-T
• gnomAD v4: 7-151253755-G-T
• MyVariant Identifiers: chr7:g.150950841G>T (hg19) ; chr7:g.151253755G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151253755G>T , CM000669.2:g.151253755G>T	GRCh38
NC_000007.13:g.150950841G>T , CM000669.1:g.150950841G>T	GRCh37
NC_000007.12:g.150581774G>T	NCBI36
NG_029468.1:g.28391C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356800.6:c.40-8084C>A	ENSP00000349254.2:n.40-8084C>A
ENST00000392811.6:c.40-8084C>A	ENSP00000376558.2:n.40-8084C>A
ENST00000469154.5:c.71-10054C>A	ENSP00000417908.1:n.71-10054C>A
ENST00000477169.5:n.184+540C>A
ENST00000491651.1:c.40-8084C>A	ENSP00000419886.1:n.40-8084C>A
NM_001003802.1:c.40-8084C>A	NP_001003802.1:n.40-8084C>A
NM_003078.3:c.40-8084C>A	NP_003069.2:n.40-8084C>A
XM_011516521.1:c.-16-10054C>A	XP_011514823.1:n.-16-10054C>A
XR_928174.1:n.717-558G>T
XM_011516521.2:c.-16-10054C>A	XP_011514823.1:n.-16-10054C>A
XM_024446887.1:c.40-8084C>A	XP_024302655.1:n.40-8084C>A
XM_024446888.1:c.-16-10054C>A	XP_024302656.1:n.-16-10054C>A
XM_024446889.1:c.-221-10054C>A	XP_024302657.1:n.-221-10054C>A
NM_003078.4:c.40-8084C>A	NP_003069.2:n.40-8084C>A
NM_001003802.2:c.40-8084C>A	NP_001003802.1:n.40-8084C>A