Canonical Allele Identifier: CA226533909

Gene: C11orf97

Linked Data

• dbSNP Id: rs906471559
• MyVariant Identifiers: chr11:g.94255175C>T (hg19) ; chr11:g.94522009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522009C>T , CM000673.2:g.94522009C>T	GRCh38
NC_000011.9:g.94255175C>T , CM000673.1:g.94255175C>T	GRCh37
NC_000011.8:g.93894823C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4322C>T MANE Select	ENSP00000490577.1:n.250+4322C>T
NM_001190462.1:c.250+4322C>T	NP_001177391.1:n.250+4322C>T
NM_001190462.2:c.250+4322C>T MANE Select	NP_001177391.1:n.250+4322C>T