Canonical Allele Identifier: CA1008376371
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1670698003

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882523T>C , CM000663.2:g.160882523T>C GRCh38
NC_000001.10:g.160852313T>C , CM000663.1:g.160852313T>C GRCh37
NC_000001.9:g.159118937T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.158-319A>G MANE Select ENSP00000323587.3:n.158-319A>G
ENST00000326245.3:c.158-319A>G ENSP00000323587.3:n.158-319A>G
NM_017625.2:c.158-319A>G NP_060095.2:n.158-319A>G
NM_017625.3:c.158-319A>G MANE Select NP_060095.2:n.158-319A>G