Canonical Allele Identifier: CA507416259

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39735117C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244477C>T , CM000681.2:g.39244477C>T	GRCh38
NC_000019.9:g.39735117C>T , CM000681.1:g.39735117C>T	GRCh37
NC_000019.8:g.44426957C>T	NCBI36
NG_042193.1:g.5495G>A
NG_055295.1:g.9380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.210G>A	ENSP00000481633.1:p.Leu70=
ENST00000413851.3:c.198G>A MANE Select	ENSP00000409000.2:p.Leu66=
ENST00000413851.2:c.198G>A	ENSP00000409000.2:p.Leu66=
ENST00000613087.4:c.210G>A	ENSP00000481633.1:p.Leu70=
NM_172139.2:c.198G>A	NP_742151.2:p.Leu66=
XM_005258765.3:c.210G>A	XP_005258822.1:p.Leu70=
XM_011526757.1:c.210G>A	XP_011525059.1:p.Leu70=
NM_001346937.1:c.210G>A	NP_001333866.1:p.Leu70=
NM_172139.3:c.198G>A	NP_742151.2:p.Leu66=
NM_172139.4:c.198G>A MANE Select	NP_742151.2:p.Leu66=
NM_001346937.2:c.210G>A	NP_001333866.1:p.Leu70=