Canonical Allele Identifier: CA2584993831

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39244599-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244602del , CM000681.2:g.39244602del	GRCh38
NC_000019.9:g.39735242del , CM000681.1:g.39735242del	GRCh37
NC_000019.8:g.44427082del	NCBI36
NG_042193.1:g.5372del
NG_055295.1:g.9257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-106del	ENSP00000481633.1:n.193-106del
ENST00000413851.3:c.181-106del MANE Select	ENSP00000409000.2:n.181-106del
ENST00000413851.2:c.181-106del	ENSP00000409000.2:n.181-106del
ENST00000613087.4:c.193-106del	ENSP00000481633.1:n.193-106del
NM_172139.2:c.181-106del	NP_742151.2:n.181-106del
XM_005258765.3:c.193-106del	XP_005258822.1:n.193-106del
XM_011526757.1:c.193-106del	XP_011525059.1:n.193-106del
NM_001346937.1:c.193-106del	NP_001333866.1:n.193-106del
NM_172139.3:c.181-106del	NP_742151.2:n.181-106del
NM_172139.4:c.181-106del MANE Select	NP_742151.2:n.181-106del
NM_001346937.2:c.193-106del	NP_001333866.1:n.193-106del