Canonical Allele Identifier: CA421605055
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851846A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882056A>G , CM000663.2:g.160882056A>G GRCh38
NC_000001.10:g.160851846A>G , CM000663.1:g.160851846A>G GRCh37
NC_000001.9:g.159118470A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.306T>C MANE Select ENSP00000323587.3:p.Ser102=
ENST00000326245.3:c.306T>C ENSP00000323587.3:p.Ser102=
ENST00000464077.1:n.240T>C
NM_017625.2:c.306T>C NP_060095.2:p.Ser102=
NM_017625.3:c.306T>C MANE Select NP_060095.2:p.Ser102=