Canonical Allele Identifier: CA169103522
Gene: SMARCD3 HGNC NCBI

Linked Data

dbSNP Id: rs17173769

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151260343T>C , CM000669.2:g.151260343T>C GRCh38
NC_000007.13:g.150957429T>C , CM000669.1:g.150957429T>C GRCh37
NC_000007.12:g.150588362T>C NCBI36
NG_029468.1:g.21803A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356800.6:c.40-14672A>G ENSP00000349254.2:n.40-14672A>G
ENST00000392811.6:c.40-14672A>G ENSP00000376558.2:n.40-14672A>G
ENST00000469154.5:c.70+14771A>G ENSP00000417908.1:n.70+14771A>G
ENST00000491651.1:c.40-14672A>G ENSP00000419886.1:n.40-14672A>G
NM_001003802.1:c.40-14672A>G NP_001003802.1:n.40-14672A>G
NM_003078.3:c.40-14672A>G NP_003069.2:n.40-14672A>G
XM_011516521.1:c.-17+14771A>G XP_011514823.1:n.-17+14771A>G
XM_011516521.2:c.-17+14771A>G XP_011514823.1:n.-17+14771A>G
XM_024446887.1:c.40-14672A>G XP_024302655.1:n.40-14672A>G
XM_024446888.1:c.-17+14771A>G XP_024302656.1:n.-17+14771A>G
XM_024446889.1:c.-222+14771A>G XP_024302657.1:n.-222+14771A>G
NM_003078.4:c.40-14672A>G NP_003069.2:n.40-14672A>G
NM_001003802.2:c.40-14672A>G NP_001003802.1:n.40-14672A>G