Canonical Allele Identifier: CA16044417

Gene: IFNL3

Linked Data

• ClinVar Variation Id: 375658
• ClinVar RCV Id: RCV000417160 ; RCV000417187 ; RCV000417140
• dbSNP Id: rs11881222
• gnomAD v2: 19-39734923-A-G
• gnomAD v3: 19-39244283-A-G
• gnomAD v4: 19-39244283-A-G
• MyVariant Identifiers: chr19:g.39734923A>G (hg19) ; chr19:g.39244283A>G (hg38)
• PubMed: PMID:19749757 ; PMID:21346780 ; PMID:22328925 ; PMID:22992668 ; PMID:23281610

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244283A>G , CM000681.2:g.39244283A>G	GRCh38
NC_000019.9:g.39734923A>G , CM000681.1:g.39734923A>G	GRCh37
NC_000019.8:g.44426763A>G	NCBI36
NG_042193.1:g.5689T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.271-126T>C	ENSP00000481633.1:n.271-126T>C
ENST00000413851.3:c.259-126T>C MANE Select	ENSP00000409000.2:n.259-126T>C
ENST00000413851.2:c.259-126T>C	ENSP00000409000.2:n.259-126T>C
ENST00000613087.4:c.271-126T>C	ENSP00000481633.1:n.271-126T>C
NM_172139.2:c.259-126T>C	NP_742151.2:n.259-126T>C
XM_005258765.3:c.271-126T>C	XP_005258822.1:n.271-126T>C
XM_011526757.1:c.271-126T>C	XP_011525059.1:n.271-126T>C
NM_001346937.1:c.271-126T>C	NP_001333866.1:n.271-126T>C
NM_172139.3:c.259-126T>C	NP_742151.2:n.259-126T>C
NM_172139.4:c.259-126T>C MANE Select	NP_742151.2:n.259-126T>C
NM_001346937.2:c.271-126T>C	NP_001333866.1:n.271-126T>C