Canonical Allele Identifier: CA682090702

Gene: C11orf97

Linked Data

• dbSNP Id: rs1281494789
• gnomAD v3: 11-94522139-C-T
• gnomAD v4: 11-94522139-C-T
• MyVariant Identifiers: chr11:g.94255305C>T (hg19) ; chr11:g.94522139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522139C>T , CM000673.2:g.94522139C>T	GRCh38
NC_000011.9:g.94255305C>T , CM000673.1:g.94255305C>T	GRCh37
NC_000011.8:g.93894953C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4452C>T MANE Select	ENSP00000490577.1:n.250+4452C>T
NM_001190462.1:c.250+4452C>T	NP_001177391.1:n.250+4452C>T
NM_001190462.2:c.250+4452C>T MANE Select	NP_001177391.1:n.250+4452C>T