Canonical Allele Identifier: CA343307047
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851756A>C (hg19) chr1:g.160881966A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881966A>C , CM000663.2:g.160881966A>C GRCh38
NC_000001.10:g.160851756A>C , CM000663.1:g.160851756A>C GRCh37
NC_000001.9:g.159118380A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.396T>G MANE Select ENSP00000323587.3:p.Asp132Glu
ENST00000326245.3:c.396T>G ENSP00000323587.3:p.Asp132Glu
ENST00000464077.1:n.330T>G
NM_017625.2:c.396T>G NP_060095.2:p.Asp132Glu
NM_017625.3:c.396T>G MANE Select NP_060095.2:p.Asp132Glu
Search 100 bp 5'
Search 100 bp 3'