Canonical Allele Identifier: CA31617242
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs750044202

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881979G>C , CM000663.2:g.160881979G>C GRCh38
NC_000001.10:g.160851769G>C , CM000663.1:g.160851769G>C GRCh37
NC_000001.9:g.159118393G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.383C>G MANE Select ENSP00000323587.3:p.Ala128Gly
ENST00000326245.3:c.383C>G ENSP00000323587.3:p.Ala128Gly
ENST00000464077.1:n.317C>G
NM_017625.2:c.383C>G NP_060095.2:p.Ala128Gly
NM_017625.3:c.383C>G MANE Select NP_060095.2:p.Ala128Gly