Canonical Allele Identifier: CA421383106
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1670692595
MyVariant Identifiers: chr1:g.160851990G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882200G>A , CM000663.2:g.160882200G>A GRCh38
NC_000001.10:g.160851990G>A , CM000663.1:g.160851990G>A GRCh37
NC_000001.9:g.159118614G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.162C>T MANE Select ENSP00000323587.3:p.Gly54=
ENST00000326245.3:c.162C>T ENSP00000323587.3:p.Gly54=
ENST00000464077.1:n.96C>T
NM_017625.2:c.162C>T NP_060095.2:p.Gly54=
NM_017625.3:c.162C>T MANE Select NP_060095.2:p.Gly54=