Canonical Allele Identifier: CA835250594

Gene: SMARCD3

Linked Data

• dbSNP Id: rs1472641717
• gnomAD v3: 7-151253858-A-G
• gnomAD v4: 7-151253858-A-G
• MyVariant Identifiers: chr7:g.150950944A>G (hg19) ; chr7:g.151253858A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151253858A>G , CM000669.2:g.151253858A>G	GRCh38
NC_000007.13:g.150950944A>G , CM000669.1:g.150950944A>G	GRCh37
NC_000007.12:g.150581877A>G	NCBI36
NG_029468.1:g.28288T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356800.6:c.40-8187T>C	ENSP00000349254.2:n.40-8187T>C
ENST00000392811.6:c.40-8187T>C	ENSP00000376558.2:n.40-8187T>C
ENST00000469154.5:c.71-10157T>C	ENSP00000417908.1:n.71-10157T>C
ENST00000477169.5:n.184+437T>C
ENST00000491651.1:c.40-8187T>C	ENSP00000419886.1:n.40-8187T>C
NM_001003802.1:c.40-8187T>C	NP_001003802.1:n.40-8187T>C
NM_003078.3:c.40-8187T>C	NP_003069.2:n.40-8187T>C
XM_011516521.1:c.-16-10157T>C	XP_011514823.1:n.-16-10157T>C
XR_928174.1:n.717-455A>G
XM_011516521.2:c.-16-10157T>C	XP_011514823.1:n.-16-10157T>C
XM_024446887.1:c.40-8187T>C	XP_024302655.1:n.40-8187T>C
XM_024446888.1:c.-16-10157T>C	XP_024302656.1:n.-16-10157T>C
XM_024446889.1:c.-221-10157T>C	XP_024302657.1:n.-221-10157T>C
NM_003078.4:c.40-8187T>C	NP_003069.2:n.40-8187T>C
NM_001003802.2:c.40-8187T>C	NP_001003802.1:n.40-8187T>C