Canonical Allele Identifier: CA343307222
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2101910234
MyVariant Identifiers: chr1:g.160851836T>G (hg19) chr1:g.160882046T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882046T>G , CM000663.2:g.160882046T>G GRCh38
NC_000001.10:g.160851836T>G , CM000663.1:g.160851836T>G GRCh37
NC_000001.9:g.159118460T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.316A>C MANE Select ENSP00000323587.3:p.Ser106Arg
ENST00000326245.3:c.316A>C ENSP00000323587.3:p.Ser106Arg
ENST00000464077.1:n.250A>C
NM_017625.2:c.316A>C NP_060095.2:p.Ser106Arg
NM_017625.3:c.316A>C MANE Select NP_060095.2:p.Ser106Arg
Search 100 bp 5'
Search 100 bp 3'