Canonical Allele Identifier: CA1752584983
Gene: SMARCD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151253875C= , CM000669.2:g.151253875C= GRCh38
NC_000007.13:g.150950961C= , CM000669.1:g.150950961C= GRCh37
NC_000007.12:g.150581894C= NCBI36
NG_029468.1:g.28271G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356800.6:c.40-8204G= ENSP00000349254.2:n.40-8204G=
ENST00000392811.6:c.40-8204G= ENSP00000376558.2:n.40-8204G=
ENST00000469154.5:c.71-10174G= ENSP00000417908.1:n.71-10174G=
ENST00000477169.5:n.184+420G=
ENST00000491651.1:c.40-8204G= ENSP00000419886.1:n.40-8204G=
NM_001003802.1:c.40-8204G= NP_001003802.1:n.40-8204G=
NM_003078.3:c.40-8204G= NP_003069.2:n.40-8204G=
XM_011516521.1:c.-16-10174G= XP_011514823.1:n.-16-10174G=
XR_928174.1:n.717-438C=
XM_011516521.2:c.-16-10174G= XP_011514823.1:n.-16-10174G=
XM_024446887.1:c.40-8204G= XP_024302655.1:n.40-8204G=
XM_024446888.1:c.-16-10174G= XP_024302656.1:n.-16-10174G=
XM_024446889.1:c.-221-10174G= XP_024302657.1:n.-221-10174G=
NM_003078.4:c.40-8204G= NP_003069.2:n.40-8204G=
NM_001003802.2:c.40-8204G= NP_001003802.1:n.40-8204G=