Canonical Allele Identifier: CA13393006

Gene: C11orf97

Linked Data

• dbSNP Id: rs616823
• gnomAD v2: 11-94255160-G-C
• gnomAD v3: 11-94521994-G-C
• gnomAD v4: 11-94521994-G-C
• MyVariant Identifiers: chr11:g.94255160G>C (hg19) ; chr11:g.94521994G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94521994G>C , CM000673.2:g.94521994G>C	GRCh38
NC_000011.9:g.94255160G>C , CM000673.1:g.94255160G>C	GRCh37
NC_000011.8:g.93894808G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4307G>C MANE Select	ENSP00000490577.1:n.250+4307G>C
NM_001190462.1:c.250+4307G>C	NP_001177391.1:n.250+4307G>C
NM_001190462.2:c.250+4307G>C MANE Select	NP_001177391.1:n.250+4307G>C