Canonical Allele Identifier: CA343307349
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1670689640
MyVariant Identifiers: chr1:g.160851895T>A (hg19) chr1:g.160882105T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882105T>A , CM000663.2:g.160882105T>A GRCh38
NC_000001.10:g.160851895T>A , CM000663.1:g.160851895T>A GRCh37
NC_000001.9:g.159118519T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.257A>T MANE Select ENSP00000323587.3:p.His86Leu
ENST00000326245.3:c.257A>T ENSP00000323587.3:p.His86Leu
ENST00000464077.1:n.191A>T
NM_017625.2:c.257A>T NP_060095.2:p.His86Leu
NM_017625.3:c.257A>T MANE Select NP_060095.2:p.His86Leu
Search 100 bp 5'
Search 100 bp 3'