Canonical Allele Identifier: CA2648717254
Gene: ITLN1 HGNC NCBI

Linked Data

gnomAD v4: 1-160881837-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881837T>G , CM000663.2:g.160881837T>G GRCh38
NC_000001.10:g.160851627T>G , CM000663.1:g.160851627T>G GRCh37
NC_000001.9:g.159118251T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+120A>C MANE Select ENSP00000323587.3:n.405+120A>C
ENST00000326245.3:c.405+120A>C ENSP00000323587.3:n.405+120A>C
ENST00000464077.1:n.339+120A>C
NM_017625.2:c.405+120A>C NP_060095.2:n.405+120A>C
NM_017625.3:c.405+120A>C MANE Select NP_060095.2:n.405+120A>C
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