Canonical Allele Identifier: CA343307368
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851905C>A (hg19) chr1:g.160882115C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882115C>A , CM000663.2:g.160882115C>A GRCh38
NC_000001.10:g.160851905C>A , CM000663.1:g.160851905C>A GRCh37
NC_000001.9:g.159118529C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.247G>T MANE Select ENSP00000323587.3:p.Ala83Ser
ENST00000326245.3:c.247G>T ENSP00000323587.3:p.Ala83Ser
ENST00000464077.1:n.181G>T
NM_017625.2:c.247G>T NP_060095.2:p.Ala83Ser
NM_017625.3:c.247G>T MANE Select NP_060095.2:p.Ala83Ser
Search 100 bp 5'
Search 100 bp 3'