Canonical Allele Identifier: CA405752143
Gene: IFNL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243700T>A , CM000681.2:g.39243700T>A GRCh38
NC_000019.9:g.39734340T>A , CM000681.1:g.39734340T>A GRCh37
NC_000019.8:g.44426180T>A NCBI36
NG_042193.1:g.6272A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.535A>T ENSP00000481633.1:p.Thr179Ser
ENST00000413851.3:c.523A>T MANE Select ENSP00000409000.2:p.Thr175Ser
ENST00000413851.2:c.523A>T ENSP00000409000.2:p.Thr175Ser
ENST00000613087.4:c.535A>T ENSP00000481633.1:p.Thr179Ser
NM_172139.2:c.523A>T NP_742151.2:p.Thr175Ser
XM_005258765.3:c.535A>T XP_005258822.1:p.Thr179Ser
XM_011526757.1:c.535A>T XP_011525059.1:p.Thr179Ser
NM_001346937.1:c.535A>T NP_001333866.1:p.Thr179Ser
NM_172139.3:c.523A>T NP_742151.2:p.Thr175Ser
NM_172139.4:c.523A>T MANE Select NP_742151.2:p.Thr175Ser
NM_001346937.2:c.535A>T NP_001333866.1:p.Thr179Ser