Canonical Allele Identifier: CA405753115

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39735128A>T (hg19) ; chr19:g.39244488A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244488A>T , CM000681.2:g.39244488A>T	GRCh38
NC_000019.9:g.39735128A>T , CM000681.1:g.39735128A>T	GRCh37
NC_000019.8:g.44426968A>T	NCBI36
NG_042193.1:g.5484T>A
NG_055295.1:g.9369T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.199T>A	ENSP00000481633.1:p.Ser67Thr
ENST00000413851.3:c.187T>A MANE Select	ENSP00000409000.2:p.Ser63Thr
ENST00000413851.2:c.187T>A	ENSP00000409000.2:p.Ser63Thr
ENST00000613087.4:c.199T>A	ENSP00000481633.1:p.Ser67Thr
NM_172139.2:c.187T>A	NP_742151.2:p.Ser63Thr
XM_005258765.3:c.199T>A	XP_005258822.1:p.Ser67Thr
XM_011526757.1:c.199T>A	XP_011525059.1:p.Ser67Thr
NM_001346937.1:c.199T>A	NP_001333866.1:p.Ser67Thr
NM_172139.3:c.187T>A	NP_742151.2:p.Ser63Thr
NM_172139.4:c.187T>A MANE Select	NP_742151.2:p.Ser63Thr
NM_001346937.2:c.199T>A	NP_001333866.1:p.Ser67Thr