Canonical Allele Identifier: CA226533987

Gene: C11orf97

Linked Data

• dbSNP Id: rs1005346107
• gnomAD v3: 11-94522172-G-A
• gnomAD v4: 11-94522172-G-A
• MyVariant Identifiers: chr11:g.94255338G>A (hg19) ; chr11:g.94522172G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522172G>A , CM000673.2:g.94522172G>A	GRCh38
NC_000011.9:g.94255338G>A , CM000673.1:g.94255338G>A	GRCh37
NC_000011.8:g.93894986G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4485G>A MANE Select	ENSP00000490577.1:n.250+4485G>A
NM_001190462.1:c.250+4485G>A	NP_001177391.1:n.250+4485G>A
NM_001190462.2:c.250+4485G>A MANE Select	NP_001177391.1:n.250+4485G>A