Canonical Allele Identifier: CA682090652
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs1400730945
gnomAD v3: 11-94522049-G-A
gnomAD v4: 11-94522049-G-A
MyVariant Identifiers: chr11:g.94255215G>A (hg19) chr11:g.94522049G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522049G>A , CM000673.2:g.94522049G>A GRCh38
NC_000011.9:g.94255215G>A , CM000673.1:g.94255215G>A GRCh37
NC_000011.8:g.93894863G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4362G>A MANE Select ENSP00000490577.1:n.250+4362G>A
NM_001190462.1:c.250+4362G>A NP_001177391.1:n.250+4362G>A
NM_001190462.2:c.250+4362G>A MANE Select NP_001177391.1:n.250+4362G>A
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