Canonical Allele Identifier: CA343307450
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851945G>C (hg19) chr1:g.160882155G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882155G>C , CM000663.2:g.160882155G>C GRCh38
NC_000001.10:g.160851945G>C , CM000663.1:g.160851945G>C GRCh37
NC_000001.9:g.159118569G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.207C>G MANE Select ENSP00000323587.3:p.Phe69Leu
ENST00000326245.3:c.207C>G ENSP00000323587.3:p.Phe69Leu
ENST00000464077.1:n.141C>G
NM_017625.2:c.207C>G NP_060095.2:p.Phe69Leu
NM_017625.3:c.207C>G MANE Select NP_060095.2:p.Phe69Leu
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