Canonical Allele Identifier: CA343307406
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851923C>T (hg19) chr1:g.160882133C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882133C>T , CM000663.2:g.160882133C>T GRCh38
NC_000001.10:g.160851923C>T , CM000663.1:g.160851923C>T GRCh37
NC_000001.9:g.159118547C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.229G>A MANE Select ENSP00000323587.3:p.Gly77Ser
ENST00000326245.3:c.229G>A ENSP00000323587.3:p.Gly77Ser
ENST00000464077.1:n.163G>A
NM_017625.2:c.229G>A NP_060095.2:p.Gly77Ser
NM_017625.3:c.229G>A MANE Select NP_060095.2:p.Gly77Ser
Search 100 bp 5'
Search 100 bp 3'