Canonical Allele Identifier: CA682090607
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs1434650606
gnomAD v3: 11-94522000-C-T
gnomAD v4: 11-94522000-C-T
MyVariant Identifiers: chr11:g.94255166C>T (hg19) chr11:g.94522000C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522000C>T , CM000673.2:g.94522000C>T GRCh38
NC_000011.9:g.94255166C>T , CM000673.1:g.94255166C>T GRCh37
NC_000011.8:g.93894814C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4313C>T MANE Select ENSP00000490577.1:n.250+4313C>T
NM_001190462.1:c.250+4313C>T NP_001177391.1:n.250+4313C>T
NM_001190462.2:c.250+4313C>T MANE Select NP_001177391.1:n.250+4313C>T
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