Canonical Allele Identifier: CA526865817
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1225290646
gnomAD v2: 1-160852000-G-A
gnomAD v4: 1-160882210-G-A
MyVariant Identifiers: chr1:g.160852000G>A (hg19) chr1:g.160882210G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882210G>A , CM000663.2:g.160882210G>A GRCh38
NC_000001.10:g.160852000G>A , CM000663.1:g.160852000G>A GRCh37
NC_000001.9:g.159118624G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.158-6C>T MANE Select ENSP00000323587.3:n.158-6C>T
ENST00000326245.3:c.158-6C>T ENSP00000323587.3:n.158-6C>T
ENST00000464077.1:n.86C>T
NM_017625.2:c.158-6C>T NP_060095.2:n.158-6C>T
NM_017625.3:c.158-6C>T MANE Select NP_060095.2:n.158-6C>T
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