Canonical Allele Identifier: CA2793219527
Gene: C11orf97 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522230T>C , CM000673.2:g.94522230T>C GRCh38
NC_000011.9:g.94255396T>C , CM000673.1:g.94255396T>C GRCh37
NC_000011.8:g.93895044T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4543T>C MANE Select ENSP00000490577.1:n.250+4543T>C
NM_001190462.1:c.250+4543T>C NP_001177391.1:n.250+4543T>C
NM_001190462.2:c.250+4543T>C MANE Select NP_001177391.1:n.250+4543T>C
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