Canonical Allele Identifier: CA993488766
Gene: SMARCA4 HGNC NCBI

Linked Data

dbSNP Id: rs2083746989

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960938T>G , CM000681.2:g.10960938T>G GRCh38
NC_000019.9:g.11071614T>G , CM000681.1:g.11071614T>G GRCh37
NC_000019.8:g.10932614T>G NCBI36
NG_011556.2:g.5017T>G
NG_011556.3:g.5007T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642726.1:c.-265T>G ENSP00000494353.1:n.-265T>G
ENST00000643549.1:c.-265T>G ENSP00000493975.1:n.-265T>G
ENST00000644737.1:c.-265T>G ENSP00000495548.1:n.-265T>G
ENST00000646484.1:c.-265T>G ENSP00000495536.1:n.-265T>G
ENST00000646693.1:c.-265T>G ENSP00000495368.1:n.-265T>G
NM_001128844.1:c.-344T>G NP_001122316.1:n.-344T>G
NM_003072.3:c.-268T>G NP_003063.2:n.-268T>G