Canonical Allele Identifier: CA421383092
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851969C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882179C>T , CM000663.2:g.160882179C>T GRCh38
NC_000001.10:g.160851969C>T , CM000663.1:g.160851969C>T GRCh37
NC_000001.9:g.159118593C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.183G>A MANE Select ENSP00000323587.3:p.Glu61=
ENST00000326245.3:c.183G>A ENSP00000323587.3:p.Glu61=
ENST00000464077.1:n.117G>A
NM_017625.2:c.183G>A NP_060095.2:p.Glu61=
NM_017625.3:c.183G>A MANE Select NP_060095.2:p.Glu61=