Canonical Allele Identifier: CA421605007
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851819T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882029T>A , CM000663.2:g.160882029T>A GRCh38
NC_000001.10:g.160851819T>A , CM000663.1:g.160851819T>A GRCh37
NC_000001.9:g.159118443T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.333A>T MANE Select ENSP00000323587.3:p.Pro111=
ENST00000326245.3:c.333A>T ENSP00000323587.3:p.Pro111=
ENST00000464077.1:n.267A>T
NM_017625.2:c.333A>T NP_060095.2:p.Pro111=
NM_017625.3:c.333A>T MANE Select NP_060095.2:p.Pro111=
Search 100 bp 5'
Search 100 bp 3'