Canonical Allele Identifier: CA345866405
Gene: SOX11 HGNC NCBI

Linked Data

dbSNP Id: rs1064794628
gnomAD v2: 2-5833152-G-A
gnomAD v3: 2-5693020-G-A
gnomAD v4: 2-5693020-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5693020G>A , CM000664.2:g.5693020G>A GRCh38
NC_000002.11:g.5833152G>A , CM000664.1:g.5833152G>A GRCh37
NC_000002.10:g.5750603G>A NCBI36
NG_050751.1:g.5354G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322002.5:c.299G>A MANE Select ENSP00000322568.3:p.Arg100Gln
ENST00000322002.4:c.299G>A ENSP00000322568.3:p.Arg100Gln
NM_003108.3:c.299G>A NP_003099.1:p.Arg100Gln
NM_003108.4:c.299G>A MANE Select NP_003099.1:p.Arg100Gln