Canonical Allele Identifier: CA226533973
Gene: C11orf97 HGNC NCBI

Linked Data

dbSNP Id: rs927122044

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522115T>G , CM000673.2:g.94522115T>G GRCh38
NC_000011.9:g.94255281T>G , CM000673.1:g.94255281T>G GRCh37
NC_000011.8:g.93894929T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4428T>G MANE Select ENSP00000490577.1:n.250+4428T>G
NM_001190462.1:c.250+4428T>G NP_001177391.1:n.250+4428T>G
NM_001190462.2:c.250+4428T>G MANE Select NP_001177391.1:n.250+4428T>G