Canonical Allele Identifier: CA2322694613
Gene: SMARCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1179905540

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960942G>A , CM000681.2:g.10960942G>A GRCh38
NC_000019.9:g.11071618G>A , CM000681.1:g.11071618G>A GRCh37
NC_000019.8:g.10932618G>A NCBI36
NG_011556.2:g.5021G>A
NG_011556.3:g.5011G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642726.1:c.-261G>A ENSP00000494353.1:n.-261G>A
ENST00000643549.1:c.-261G>A ENSP00000493975.1:n.-261G>A
ENST00000644737.1:c.-261G>A ENSP00000495548.1:n.-261G>A
ENST00000646484.1:c.-261G>A ENSP00000495536.1:n.-261G>A
ENST00000646693.1:c.-261G>A ENSP00000495368.1:n.-261G>A
NM_001128844.1:c.-340G>A NP_001122316.1:n.-340G>A
NM_003072.3:c.-264G>A NP_003063.2:n.-264G>A