Canonical Allele Identifier: CA890138690
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1202183933
MyVariant Identifiers: chr1:g.160851573C>T (hg19) chr1:g.160881783C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881783C>T , CM000663.2:g.160881783C>T GRCh38
NC_000001.10:g.160851573C>T , CM000663.1:g.160851573C>T GRCh37
NC_000001.9:g.159118197C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+174G>A MANE Select ENSP00000323587.3:n.405+174G>A
ENST00000326245.3:c.405+174G>A ENSP00000323587.3:n.405+174G>A
ENST00000464077.1:n.339+174G>A
NM_017625.2:c.405+174G>A NP_060095.2:n.405+174G>A
NM_017625.3:c.405+174G>A MANE Select NP_060095.2:n.405+174G>A
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