Canonical Allele Identifier: CA405753118
Gene: IFNL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39244490T>C , CM000681.2:g.39244490T>C GRCh38
NC_000019.9:g.39735130T>C , CM000681.1:g.39735130T>C GRCh37
NC_000019.8:g.44426970T>C NCBI36
NG_042193.1:g.5482A>G
NG_055295.1:g.9367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.197A>G ENSP00000481633.1:p.Glu66Gly
ENST00000413851.3:c.185A>G MANE Select ENSP00000409000.2:p.Glu62Gly
ENST00000413851.2:c.185A>G ENSP00000409000.2:p.Glu62Gly
ENST00000613087.4:c.197A>G ENSP00000481633.1:p.Glu66Gly
NM_172139.2:c.185A>G NP_742151.2:p.Glu62Gly
XM_005258765.3:c.197A>G XP_005258822.1:p.Glu66Gly
XM_011526757.1:c.197A>G XP_011525059.1:p.Glu66Gly
NM_001346937.1:c.197A>G NP_001333866.1:p.Glu66Gly
NM_172139.3:c.185A>G NP_742151.2:p.Glu62Gly
NM_172139.4:c.185A>G MANE Select NP_742151.2:p.Glu62Gly
NM_001346937.2:c.197A>G NP_001333866.1:p.Glu66Gly