Canonical Allele Identifier: CA526865833
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1426166199
gnomAD v2: 1-160852366-A-T
gnomAD v3: 1-160882576-A-T
gnomAD v4: 1-160882576-A-T
MyVariant Identifiers: chr1:g.160852366A>T (hg19) chr1:g.160882576A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882576A>T , CM000663.2:g.160882576A>T GRCh38
NC_000001.10:g.160852366A>T , CM000663.1:g.160852366A>T GRCh37
NC_000001.9:g.159118990A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.158-372T>A MANE Select ENSP00000323587.3:n.158-372T>A
ENST00000326245.3:c.158-372T>A ENSP00000323587.3:n.158-372T>A
NM_017625.2:c.158-372T>A NP_060095.2:n.158-372T>A
NM_017625.3:c.158-372T>A MANE Select NP_060095.2:n.158-372T>A
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