Canonical Allele Identifier: CA405753083
Gene: IFNL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39244470A>T , CM000681.2:g.39244470A>T GRCh38
NC_000019.9:g.39735110A>T , CM000681.1:g.39735110A>T GRCh37
NC_000019.8:g.44426950A>T NCBI36
NG_042193.1:g.5502T>A
NG_055295.1:g.9387T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.217T>A ENSP00000481633.1:p.Cys73Ser
ENST00000413851.3:c.205T>A MANE Select ENSP00000409000.2:p.Cys69Ser
ENST00000413851.2:c.205T>A ENSP00000409000.2:p.Cys69Ser
ENST00000613087.4:c.217T>A ENSP00000481633.1:p.Cys73Ser
NM_172139.2:c.205T>A NP_742151.2:p.Cys69Ser
XM_005258765.3:c.217T>A XP_005258822.1:p.Cys73Ser
XM_011526757.1:c.217T>A XP_011525059.1:p.Cys73Ser
NM_001346937.1:c.217T>A NP_001333866.1:p.Cys73Ser
NM_172139.3:c.205T>A NP_742151.2:p.Cys69Ser
NM_172139.4:c.205T>A MANE Select NP_742151.2:p.Cys69Ser
NM_001346937.2:c.217T>A NP_001333866.1:p.Cys73Ser