Canonical Allele Identifier: CA405752137

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39734336A>G (hg19) ; chr19:g.39243696A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243696A>G , CM000681.2:g.39243696A>G	GRCh38
NC_000019.9:g.39734336A>G , CM000681.1:g.39734336A>G	GRCh37
NC_000019.8:g.44426176A>G	NCBI36
NG_042193.1:g.6276T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.539T>C	ENSP00000481633.1:p.Phe180Ser
ENST00000413851.3:c.527T>C MANE Select	ENSP00000409000.2:p.Phe176Ser
ENST00000413851.2:c.527T>C	ENSP00000409000.2:p.Phe176Ser
ENST00000613087.4:c.539T>C	ENSP00000481633.1:p.Phe180Ser
NM_172139.2:c.527T>C	NP_742151.2:p.Phe176Ser
XM_005258765.3:c.539T>C	XP_005258822.1:p.Phe180Ser
XM_011526757.1:c.539T>C	XP_011525059.1:p.Phe180Ser
NM_001346937.1:c.539T>C	NP_001333866.1:p.Phe180Ser
NM_172139.3:c.527T>C	NP_742151.2:p.Phe176Ser
NM_172139.4:c.527T>C MANE Select	NP_742151.2:p.Phe176Ser
NM_001346937.2:c.539T>C	NP_001333866.1:p.Phe180Ser