Canonical Allele Identifier: CA421605259
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1386115711

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882173A>G , CM000663.2:g.160882173A>G GRCh38
NC_000001.10:g.160851963A>G , CM000663.1:g.160851963A>G GRCh37
NC_000001.9:g.159118587A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.189T>C MANE Select ENSP00000323587.3:p.Gly63=
ENST00000326245.3:c.189T>C ENSP00000323587.3:p.Gly63=
ENST00000464077.1:n.123T>C
NM_017625.2:c.189T>C NP_060095.2:p.Gly63=
NM_017625.3:c.189T>C MANE Select NP_060095.2:p.Gly63=