Canonical Allele Identifier: CA882116954

Gene: IFNL3

Linked Data

• dbSNP Id: rs1469707185
• gnomAD v3: 19-39244619-CTCT-C
• gnomAD v4: 19-39244619-CTCT-C
• MyVariant Identifiers: chr19:g.39735260_39735262del (hg19) ; chr19:g.39244620_39244622del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244625_39244627del , CM000681.2:g.39244625_39244627del	GRCh38
NC_000019.9:g.39735265_39735267del , CM000681.1:g.39735265_39735267del	GRCh37
NC_000019.8:g.44427105_44427107del	NCBI36
NG_042193.1:g.5350_5352del
NG_055295.1:g.9235_9237del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-128_193-126del	ENSP00000481633.1:n.193-128_193-126del
ENST00000413851.3:c.181-128_181-126del MANE Select	ENSP00000409000.2:n.181-128_181-126del
ENST00000413851.2:c.181-128_181-126del	ENSP00000409000.2:n.181-128_181-126del
ENST00000613087.4:c.193-128_193-126del	ENSP00000481633.1:n.193-128_193-126del
NM_172139.2:c.181-128_181-126del	NP_742151.2:n.181-128_181-126del
XM_005258765.3:c.193-128_193-126del	XP_005258822.1:n.193-128_193-126del
XM_011526757.1:c.193-128_193-126del	XP_011525059.1:n.193-128_193-126del
NM_001346937.1:c.193-128_193-126del	NP_001333866.1:n.193-128_193-126del
NM_172139.3:c.181-128_181-126del	NP_742151.2:n.181-128_181-126del
NM_172139.4:c.181-128_181-126del MANE Select	NP_742151.2:n.181-128_181-126del
NM_001346937.2:c.193-128_193-126del	NP_001333866.1:n.193-128_193-126del