Canonical Allele Identifier: CA421605014
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851825G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882035G>T , CM000663.2:g.160882035G>T GRCh38
NC_000001.10:g.160851825G>T , CM000663.1:g.160851825G>T GRCh37
NC_000001.9:g.159118449G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.327C>A MANE Select ENSP00000323587.3:p.Val109=
ENST00000326245.3:c.327C>A ENSP00000323587.3:p.Val109=
ENST00000464077.1:n.261C>A
NM_017625.2:c.327C>A NP_060095.2:p.Val109=
NM_017625.3:c.327C>A MANE Select NP_060095.2:p.Val109=
Search 100 bp 5'
Search 100 bp 3'