Canonical Allele Identifier: CA1992462689
Gene: C11orf97 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522186T= , CM000673.2:g.94522186T= GRCh38
NC_000011.9:g.94255352T= , CM000673.1:g.94255352T= GRCh37
NC_000011.8:g.93895000T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4499T= MANE Select ENSP00000490577.1:n.250+4499T=
NM_001190462.1:c.250+4499T= NP_001177391.1:n.250+4499T=
NM_001190462.2:c.250+4499T= MANE Select NP_001177391.1:n.250+4499T=
Search 100 bp 5'
Search 100 bp 3'