Canonical Allele Identifier: CA343307120
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851791T>C (hg19) chr1:g.160882001T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882001T>C , CM000663.2:g.160882001T>C GRCh38
NC_000001.10:g.160851791T>C , CM000663.1:g.160851791T>C GRCh37
NC_000001.9:g.159118415T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.361A>G MANE Select ENSP00000323587.3:p.Asn121Asp
ENST00000326245.3:c.361A>G ENSP00000323587.3:p.Asn121Asp
ENST00000464077.1:n.295A>G
NM_017625.2:c.361A>G NP_060095.2:p.Asn121Asp
NM_017625.3:c.361A>G MANE Select NP_060095.2:p.Asn121Asp
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