Canonical Allele Identifier: CA343307168
Gene: ITLN1 HGNC NCBI

Linked Data

gnomAD v4: 1-160882021-T-A
MyVariant Identifiers: chr1:g.160851811T>A (hg19) chr1:g.160882021T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882021T>A , CM000663.2:g.160882021T>A GRCh38
NC_000001.10:g.160851811T>A , CM000663.1:g.160851811T>A GRCh37
NC_000001.9:g.159118435T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.341A>T MANE Select ENSP00000323587.3:p.Asp114Val
ENST00000326245.3:c.341A>T ENSP00000323587.3:p.Asp114Val
ENST00000464077.1:n.275A>T
NM_017625.2:c.341A>T NP_060095.2:p.Asp114Val
NM_017625.3:c.341A>T MANE Select NP_060095.2:p.Asp114Val
Search 100 bp 5'
Search 100 bp 3'