Canonical Allele Identifier: CA600840132

Gene: C11orf97

Linked Data

• dbSNP Id: rs1312950183
• gnomAD v2: 11-94255187-A-G
• gnomAD v3: 11-94522021-A-G
• gnomAD v4: 11-94522021-A-G
• MyVariant Identifiers: chr11:g.94255187A>G (hg19) ; chr11:g.94522021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522021A>G , CM000673.2:g.94522021A>G	GRCh38
NC_000011.9:g.94255187A>G , CM000673.1:g.94255187A>G	GRCh37
NC_000011.8:g.93894835A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4334A>G MANE Select	ENSP00000490577.1:n.250+4334A>G
NM_001190462.1:c.250+4334A>G	NP_001177391.1:n.250+4334A>G
NM_001190462.2:c.250+4334A>G MANE Select	NP_001177391.1:n.250+4334A>G