Canonical Allele Identifier: CA600840233
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs1278701062
gnomAD v2: 11-94255294-T-C
gnomAD v3: 11-94522128-T-C
gnomAD v4: 11-94522128-T-C
MyVariant Identifiers: chr11:g.94255294T>C (hg19) chr11:g.94522128T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522128T>C , CM000673.2:g.94522128T>C GRCh38
NC_000011.9:g.94255294T>C , CM000673.1:g.94255294T>C GRCh37
NC_000011.8:g.93894942T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4441T>C MANE Select ENSP00000490577.1:n.250+4441T>C
NM_001190462.1:c.250+4441T>C NP_001177391.1:n.250+4441T>C
NM_001190462.2:c.250+4441T>C MANE Select NP_001177391.1:n.250+4441T>C
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