Canonical Allele Identifier: CA882116689

Gene: IFNL3

Linked Data

• dbSNP Id: rs1234868266
• gnomAD v4: 19-39244337-AAGG-A
• MyVariant Identifiers: chr19:g.39734978_39734980del (hg19) ; chr19:g.39244338_39244340del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244340_39244342del , CM000681.2:g.39244340_39244342del	GRCh38
NC_000019.9:g.39734980_39734982del , CM000681.1:g.39734980_39734982del	GRCh37
NC_000019.8:g.44426820_44426822del	NCBI36
NG_042193.1:g.5632_5634del
NG_055295.1:g.9517_9519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.270+77_270+79del	ENSP00000481633.1:n.270+77_270+79del
ENST00000413851.3:c.258+77_258+79del MANE Select	ENSP00000409000.2:n.258+77_258+79del
ENST00000413851.2:c.258+77_258+79del	ENSP00000409000.2:n.258+77_258+79del
ENST00000613087.4:c.270+77_270+79del	ENSP00000481633.1:n.270+77_270+79del
NM_172139.2:c.258+77_258+79del	NP_742151.2:n.258+77_258+79del
XM_005258765.3:c.270+77_270+79del	XP_005258822.1:n.270+77_270+79del
XM_011526757.1:c.270+77_270+79del	XP_011525059.1:n.270+77_270+79del
NM_001346937.1:c.270+77_270+79del	NP_001333866.1:n.270+77_270+79del
NM_172139.3:c.258+77_258+79del	NP_742151.2:n.258+77_258+79del
NM_172139.4:c.258+77_258+79del MANE Select	NP_742151.2:n.258+77_258+79del
NM_001346937.2:c.270+77_270+79del	NP_001333866.1:n.270+77_270+79del