Canonical Allele Identifier: CA2322694666
Gene: SMARCA4 HGNC NCBI

Linked Data

dbSNP Id: rs2083749777

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960986G>A , CM000681.2:g.10960986G>A GRCh38
NC_000019.9:g.11071662G>A , CM000681.1:g.11071662G>A GRCh37
NC_000019.8:g.10932662G>A NCBI36
NG_011556.2:g.5065G>A
NG_011556.3:g.5055G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000711079.1:c.-220G>A ENSP00000518564.1:n.-220G>A
ENST00000642628.1:c.-220G>A ENSP00000496498.1:n.-220G>A
ENST00000642726.1:c.-217G>A ENSP00000494353.1:n.-217G>A
ENST00000643296.1:c.-220G>A ENSP00000496635.1:n.-220G>A
ENST00000643549.1:c.-217G>A ENSP00000493975.1:n.-217G>A
ENST00000644737.1:c.-217G>A ENSP00000495548.1:n.-217G>A
ENST00000646484.1:c.-217G>A ENSP00000495536.1:n.-217G>A
ENST00000646693.1:c.-217G>A ENSP00000495368.1:n.-217G>A
ENST00000647230.1:c.-220G>A ENSP00000494676.1:n.-220G>A
NM_001128844.1:c.-296G>A NP_001122316.1:n.-296G>A
NM_003072.3:c.-220G>A NP_003063.2:n.-220G>A