Canonical Allele Identifier: CA343307254
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851850G>T (hg19) chr1:g.160882060G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882060G>T , CM000663.2:g.160882060G>T GRCh38
NC_000001.10:g.160851850G>T , CM000663.1:g.160851850G>T GRCh37
NC_000001.9:g.159118474G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.302C>A MANE Select ENSP00000323587.3:p.Ser101Tyr
ENST00000326245.3:c.302C>A ENSP00000323587.3:p.Ser101Tyr
ENST00000464077.1:n.236C>A
NM_017625.2:c.302C>A NP_060095.2:p.Ser101Tyr
NM_017625.3:c.302C>A MANE Select NP_060095.2:p.Ser101Tyr
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