Canonical Allele Identifier: CA405753110

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39735125G>T (hg19) ; chr19:g.39244485G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244485G>T , CM000681.2:g.39244485G>T	GRCh38
NC_000019.9:g.39735125G>T , CM000681.1:g.39735125G>T	GRCh37
NC_000019.8:g.44426965G>T	NCBI36
NG_042193.1:g.5487C>A
NG_055295.1:g.9372C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.202C>A	ENSP00000481633.1:p.Leu68Ile
ENST00000413851.3:c.190C>A MANE Select	ENSP00000409000.2:p.Leu64Ile
ENST00000413851.2:c.190C>A	ENSP00000409000.2:p.Leu64Ile
ENST00000613087.4:c.202C>A	ENSP00000481633.1:p.Leu68Ile
NM_172139.2:c.190C>A	NP_742151.2:p.Leu64Ile
XM_005258765.3:c.202C>A	XP_005258822.1:p.Leu68Ile
XM_011526757.1:c.202C>A	XP_011525059.1:p.Leu68Ile
NM_001346937.1:c.202C>A	NP_001333866.1:p.Leu68Ile
NM_172139.3:c.190C>A	NP_742151.2:p.Leu64Ile
NM_172139.4:c.190C>A MANE Select	NP_742151.2:p.Leu64Ile
NM_001346937.2:c.202C>A	NP_001333866.1:p.Leu68Ile