Canonical Allele Identifier: CA682090685
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs545757298
MyVariant Identifiers: chr11:g.94255291C>A (hg19) chr11:g.94522125C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522125C>A , CM000673.2:g.94522125C>A GRCh38
NC_000011.9:g.94255291C>A , CM000673.1:g.94255291C>A GRCh37
NC_000011.8:g.93894939C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4438C>A MANE Select ENSP00000490577.1:n.250+4438C>A
NM_001190462.1:c.250+4438C>A NP_001177391.1:n.250+4438C>A
NM_001190462.2:c.250+4438C>A MANE Select NP_001177391.1:n.250+4438C>A
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