Canonical Allele Identifier: CA31617607
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs11265508

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882335C>T , CM000663.2:g.160882335C>T GRCh38
NC_000001.10:g.160852125C>T , CM000663.1:g.160852125C>T GRCh37
NC_000001.9:g.159118749C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.158-131G>A MANE Select ENSP00000323587.3:n.158-131G>A
ENST00000326245.3:c.158-131G>A ENSP00000323587.3:n.158-131G>A
NM_017625.2:c.158-131G>A NP_060095.2:n.158-131G>A
NM_017625.3:c.158-131G>A MANE Select NP_060095.2:n.158-131G>A