Canonical Allele Identifier: CA343307105
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851784A>T (hg19) chr1:g.160881994A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881994A>T , CM000663.2:g.160881994A>T GRCh38
NC_000001.10:g.160851784A>T , CM000663.1:g.160851784A>T GRCh37
NC_000001.9:g.159118408A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.368T>A MANE Select ENSP00000323587.3:p.Phe123Tyr
ENST00000326245.3:c.368T>A ENSP00000323587.3:p.Phe123Tyr
ENST00000464077.1:n.302T>A
NM_017625.2:c.368T>A NP_060095.2:p.Phe123Tyr
NM_017625.3:c.368T>A MANE Select NP_060095.2:p.Phe123Tyr
Search 100 bp 5'
Search 100 bp 3'