Canonical Allele Identifier: CA882116939

Gene: IFNL3

Linked Data

• dbSNP Id: rs1420287397
• MyVariant Identifiers: chr19:g.39735219_39735220insT (hg19) ; chr19:g.39244579_39244580insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244579_39244580insT , CM000681.2:g.39244579_39244580insT	GRCh38
NC_000019.9:g.39735219_39735220insT , CM000681.1:g.39735219_39735220insT	GRCh37
NC_000019.8:g.44427059_44427060insT	NCBI36
NG_042193.1:g.5392_5393insA
NG_055295.1:g.9277_9278insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-86_193-85insA	ENSP00000481633.1:n.193-86_193-85insA
ENST00000413851.3:c.181-86_181-85insA MANE Select	ENSP00000409000.2:n.181-86_181-85insA
ENST00000413851.2:c.181-86_181-85insA	ENSP00000409000.2:n.181-86_181-85insA
ENST00000613087.4:c.193-86_193-85insA	ENSP00000481633.1:n.193-86_193-85insA
NM_172139.2:c.181-86_181-85insA	NP_742151.2:n.181-86_181-85insA
XM_005258765.3:c.193-86_193-85insA	XP_005258822.1:n.193-86_193-85insA
XM_011526757.1:c.193-86_193-85insA	XP_011525059.1:n.193-86_193-85insA
NM_001346937.1:c.193-86_193-85insA	NP_001333866.1:n.193-86_193-85insA
NM_172139.3:c.181-86_181-85insA	NP_742151.2:n.181-86_181-85insA
NM_172139.4:c.181-86_181-85insA MANE Select	NP_742151.2:n.181-86_181-85insA
NM_001346937.2:c.193-86_193-85insA	NP_001333866.1:n.193-86_193-85insA