Canonical Allele Identifier: CA226533974
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs527608552
gnomAD v3: 11-94522124-A-C
gnomAD v4: 11-94522124-A-C
MyVariant Identifiers: chr11:g.94255290A>C (hg19) chr11:g.94522124A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522124A>C , CM000673.2:g.94522124A>C GRCh38
NC_000011.9:g.94255290A>C , CM000673.1:g.94255290A>C GRCh37
NC_000011.8:g.93894938A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4437A>C MANE Select ENSP00000490577.1:n.250+4437A>C
NM_001190462.1:c.250+4437A>C NP_001177391.1:n.250+4437A>C
NM_001190462.2:c.250+4437A>C MANE Select NP_001177391.1:n.250+4437A>C
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