Canonical Allele Identifier: CA2584993880

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39244671-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244671C>A , CM000681.2:g.39244671C>A	GRCh38
NC_000019.9:g.39735311C>A , CM000681.1:g.39735311C>A	GRCh37
NC_000019.8:g.44427151C>A	NCBI36
NG_042193.1:g.5301G>T
NG_055295.1:g.9186G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.192+117G>T	ENSP00000481633.1:n.192+117G>T
ENST00000413851.3:c.180+117G>T MANE Select	ENSP00000409000.2:n.180+117G>T
ENST00000413851.2:c.180+117G>T	ENSP00000409000.2:n.180+117G>T
ENST00000613087.4:c.192+117G>T	ENSP00000481633.1:n.192+117G>T
NM_172139.2:c.180+117G>T	NP_742151.2:n.180+117G>T
XM_005258765.3:c.192+117G>T	XP_005258822.1:n.192+117G>T
XM_011526757.1:c.192+117G>T	XP_011525059.1:n.192+117G>T
NM_001346937.1:c.192+117G>T	NP_001333866.1:n.192+117G>T
NM_172139.3:c.180+117G>T	NP_742151.2:n.180+117G>T
NM_172139.4:c.180+117G>T MANE Select	NP_742151.2:n.180+117G>T
NM_001346937.2:c.192+117G>T	NP_001333866.1:n.192+117G>T