Canonical Allele Identifier: CA169154992

Gene: SMARCD3

Linked Data

• dbSNP Id: rs923063892
• MyVariant Identifiers: chr7:g.150950969T>C (hg19) ; chr7:g.151253883T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151253883T>C , CM000669.2:g.151253883T>C	GRCh38
NC_000007.13:g.150950969T>C , CM000669.1:g.150950969T>C	GRCh37
NC_000007.12:g.150581902T>C	NCBI36
NG_029468.1:g.28263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356800.6:c.40-8212A>G	ENSP00000349254.2:n.40-8212A>G
ENST00000392811.6:c.40-8212A>G	ENSP00000376558.2:n.40-8212A>G
ENST00000469154.5:c.71-10182A>G	ENSP00000417908.1:n.71-10182A>G
ENST00000477169.5:n.184+412A>G
ENST00000491651.1:c.40-8212A>G	ENSP00000419886.1:n.40-8212A>G
NM_001003802.1:c.40-8212A>G	NP_001003802.1:n.40-8212A>G
NM_003078.3:c.40-8212A>G	NP_003069.2:n.40-8212A>G
XM_011516521.1:c.-16-10182A>G	XP_011514823.1:n.-16-10182A>G
XR_928174.1:n.717-430T>C
XM_011516521.2:c.-16-10182A>G	XP_011514823.1:n.-16-10182A>G
XM_024446887.1:c.40-8212A>G	XP_024302655.1:n.40-8212A>G
XM_024446888.1:c.-16-10182A>G	XP_024302656.1:n.-16-10182A>G
XM_024446889.1:c.-221-10182A>G	XP_024302657.1:n.-221-10182A>G
NM_003078.4:c.40-8212A>G	NP_003069.2:n.40-8212A>G
NM_001003802.2:c.40-8212A>G	NP_001003802.1:n.40-8212A>G