Canonical Allele Identifier: CA993488754
Gene: SMARCA4 HGNC NCBI

Linked Data

dbSNP Id: rs2083746539

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960928G>A , CM000681.2:g.10960928G>A GRCh38
NC_000019.9:g.11071604G>A , CM000681.1:g.11071604G>A GRCh37
NC_000019.8:g.10932604G>A NCBI36
NG_011556.2:g.5007G>A
NG_011556.3:g.4997G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001128844.1:c.-354G>A NP_001122316.1:n.-354G>A
NM_003072.3:c.-278G>A NP_003063.2:n.-278G>A