Canonical Allele Identifier: CA2648717442
Gene: ITLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882316T>C , CM000663.2:g.160882316T>C GRCh38
NC_000001.10:g.160852106T>C , CM000663.1:g.160852106T>C GRCh37
NC_000001.9:g.159118730T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.158-112A>G MANE Select ENSP00000323587.3:n.158-112A>G
ENST00000326245.3:c.158-112A>G ENSP00000323587.3:n.158-112A>G
NM_017625.2:c.158-112A>G NP_060095.2:n.158-112A>G
NM_017625.3:c.158-112A>G MANE Select NP_060095.2:n.158-112A>G