Canonical Allele Identifier: CA421605151
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs142720493
gnomAD v2: 1-160851921-G-T
gnomAD v4: 1-160882131-G-T
MyVariant Identifiers: chr1:g.160851921G>T (hg19) chr1:g.160882131G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882131G>T , CM000663.2:g.160882131G>T GRCh38
NC_000001.10:g.160851921G>T , CM000663.1:g.160851921G>T GRCh37
NC_000001.9:g.159118545G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.231C>A MANE Select ENSP00000323587.3:p.Gly77=
ENST00000326245.3:c.231C>A ENSP00000323587.3:p.Gly77=
ENST00000464077.1:n.165C>A
NM_017625.2:c.231C>A NP_060095.2:p.Gly77=
NM_017625.3:c.231C>A MANE Select NP_060095.2:p.Gly77=
Search 100 bp 5'
Search 100 bp 3'