Canonical Allele Identifier: CA995803284

Gene: IFNL3

Linked Data

• dbSNP Id: rs2074935065
• gnomAD v3: 19-39244620-T-G
• gnomAD v4: 19-39244620-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244620T>G , CM000681.2:g.39244620T>G	GRCh38
NC_000019.9:g.39735260T>G , CM000681.1:g.39735260T>G	GRCh37
NC_000019.8:g.44427100T>G	NCBI36
NG_042193.1:g.5352A>C
NG_055295.1:g.9237A>C

Transcript Alleles

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