Canonical Allele Identifier: CA2322694662
Gene: SMARCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1444675155

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960985G>C , CM000681.2:g.10960985G>C GRCh38
NC_000019.9:g.11071661G>C , CM000681.1:g.11071661G>C GRCh37
NC_000019.8:g.10932661G>C NCBI36
NG_011556.2:g.5064G>C
NG_011556.3:g.5054G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000711079.1:c.-221G>C ENSP00000518564.1:n.-221G>C
ENST00000642628.1:c.-221G>C ENSP00000496498.1:n.-221G>C
ENST00000642726.1:c.-218G>C ENSP00000494353.1:n.-218G>C
ENST00000643296.1:c.-221G>C ENSP00000496635.1:n.-221G>C
ENST00000643549.1:c.-218G>C ENSP00000493975.1:n.-218G>C
ENST00000644737.1:c.-218G>C ENSP00000495548.1:n.-218G>C
ENST00000646484.1:c.-218G>C ENSP00000495536.1:n.-218G>C
ENST00000646693.1:c.-218G>C ENSP00000495368.1:n.-218G>C
ENST00000647230.1:c.-221G>C ENSP00000494676.1:n.-221G>C
NM_001128844.1:c.-297G>C NP_001122316.1:n.-297G>C
NM_003072.3:c.-221G>C NP_003063.2:n.-221G>C