Canonical Allele Identifier: CA13393007

Gene: C11orf97

Linked Data

• dbSNP Id: rs16924603
• gnomAD v2: 11-94255259-T-C
• gnomAD v3: 11-94522093-T-C
• gnomAD v4: 11-94522093-T-C
• MyVariant Identifiers: chr11:g.94255259T>C (hg19) ; chr11:g.94522093T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522093T>C , CM000673.2:g.94522093T>C	GRCh38
NC_000011.9:g.94255259T>C , CM000673.1:g.94255259T>C	GRCh37
NC_000011.8:g.93894907T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000542198.3:c.250+4406T>C MANE Select	ENSP00000490577.1:n.250+4406T>C
NM_001190462.1:c.250+4406T>C	NP_001177391.1:n.250+4406T>C
NM_001190462.2:c.250+4406T>C MANE Select	NP_001177391.1:n.250+4406T>C