Canonical Allele Identifier: CA1202733
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs770294515

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882182A>G , CM000663.2:g.160882182A>G GRCh38
NC_000001.10:g.160851972A>G , CM000663.1:g.160851972A>G GRCh37
NC_000001.9:g.159118596A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.180T>C MANE Select ENSP00000323587.3:p.Thr60=
ENST00000326245.3:c.180T>C ENSP00000323587.3:p.Thr60=
ENST00000464077.1:n.114T>C
NM_017625.2:c.180T>C NP_060095.2:p.Thr60=
NM_017625.3:c.180T>C MANE Select NP_060095.2:p.Thr60=