Canonical Allele Identifier: CA941031537
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs1947662010
gnomAD v3: 11-94522134-A-G
gnomAD v4: 11-94522134-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522134A>G , CM000673.2:g.94522134A>G GRCh38
NC_000011.9:g.94255300A>G , CM000673.1:g.94255300A>G GRCh37
NC_000011.8:g.93894948A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4447A>G MANE Select ENSP00000490577.1:n.250+4447A>G
NM_001190462.1:c.250+4447A>G NP_001177391.1:n.250+4447A>G
NM_001190462.2:c.250+4447A>G MANE Select NP_001177391.1:n.250+4447A>G
Search 100 bp 5'
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