Canonical Allele Identifier: CA920107224

Gene: IFNL3

Linked Data

• dbSNP Id: rs1600453512
• gnomAD v4: 19-39244583-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244587del , CM000681.2:g.39244587del	GRCh38
NC_000019.9:g.39735227del , CM000681.1:g.39735227del	GRCh37
NC_000019.8:g.44427067del	NCBI36
NG_042193.1:g.5388del
NG_055295.1:g.9273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-90del	ENSP00000481633.1:n.193-90del
ENST00000413851.3:c.181-90del MANE Select	ENSP00000409000.2:n.181-90del
ENST00000413851.2:c.181-90del	ENSP00000409000.2:n.181-90del
ENST00000613087.4:c.193-90del	ENSP00000481633.1:n.193-90del
NM_172139.2:c.181-90del	NP_742151.2:n.181-90del
XM_005258765.3:c.193-90del	XP_005258822.1:n.193-90del
XM_011526757.1:c.193-90del	XP_011525059.1:n.193-90del
NM_001346937.1:c.193-90del	NP_001333866.1:n.193-90del
NM_172139.3:c.181-90del	NP_742151.2:n.181-90del
NM_172139.4:c.181-90del MANE Select	NP_742151.2:n.181-90del
NM_001346937.2:c.193-90del	NP_001333866.1:n.193-90del