Canonical Allele Identifier: CA1008376118
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1571142541
gnomAD v3: 1-160881865-A-C
gnomAD v4: 1-160881865-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881865A>C , CM000663.2:g.160881865A>C GRCh38
NC_000001.10:g.160851655A>C , CM000663.1:g.160851655A>C GRCh37
NC_000001.9:g.159118279A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+92T>G MANE Select ENSP00000323587.3:n.405+92T>G
ENST00000326245.3:c.405+92T>G ENSP00000323587.3:n.405+92T>G
ENST00000464077.1:n.339+92T>G
NM_017625.2:c.405+92T>G NP_060095.2:n.405+92T>G
NM_017625.3:c.405+92T>G MANE Select NP_060095.2:n.405+92T>G
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