Canonical Allele Identifier: CA2584993795

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39244550-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244551dup , CM000681.2:g.39244551dup	GRCh38
NC_000019.9:g.39735191dup , CM000681.1:g.39735191dup	GRCh37
NC_000019.8:g.44427031dup	NCBI36
NG_042193.1:g.5421dup
NG_055295.1:g.9306dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-57dup	ENSP00000481633.1:n.193-57dup
ENST00000413851.3:c.181-57dup MANE Select	ENSP00000409000.2:n.181-57dup
ENST00000413851.2:c.181-57dup	ENSP00000409000.2:n.181-57dup
ENST00000613087.4:c.193-57dup	ENSP00000481633.1:n.193-57dup
NM_172139.2:c.181-57dup	NP_742151.2:n.181-57dup
XM_005258765.3:c.193-57dup	XP_005258822.1:n.193-57dup
XM_011526757.1:c.193-57dup	XP_011525059.1:n.193-57dup
NM_001346937.1:c.193-57dup	NP_001333866.1:n.193-57dup
NM_172139.3:c.181-57dup	NP_742151.2:n.181-57dup
NM_172139.4:c.181-57dup MANE Select	NP_742151.2:n.181-57dup
NM_001346937.2:c.193-57dup	NP_001333866.1:n.193-57dup