Canonical Allele Identifier: CA31617632

Gene: ITLN1

Linked Data

• dbSNP Id: rs1000396540
• MyVariant Identifiers: chr1:g.160852169C>T (hg19) ; chr1:g.160882379C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882379C>T , CM000663.2:g.160882379C>T	GRCh38
NC_000001.10:g.160852169C>T , CM000663.1:g.160852169C>T	GRCh37
NC_000001.9:g.159118793C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326245.4:c.158-175G>A MANE Select	ENSP00000323587.3:n.158-175G>A
ENST00000326245.3:c.158-175G>A	ENSP00000323587.3:n.158-175G>A
NM_017625.2:c.158-175G>A	NP_060095.2:n.158-175G>A
NM_017625.3:c.158-175G>A MANE Select	NP_060095.2:n.158-175G>A