Canonical Allele Identifier: CA995803295

Gene: IFNL3

Linked Data

• dbSNP Id: rs2074935418
• gnomAD v3: 19-39244662-T-C
• gnomAD v4: 19-39244662-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244662T>C , CM000681.2:g.39244662T>C	GRCh38
NC_000019.9:g.39735302T>C , CM000681.1:g.39735302T>C	GRCh37
NC_000019.8:g.44427142T>C	NCBI36
NG_042193.1:g.5310A>G
NG_055295.1:g.9195A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.192+126A>G	ENSP00000481633.1:n.192+126A>G
ENST00000413851.3:c.180+126A>G MANE Select	ENSP00000409000.2:n.180+126A>G
ENST00000413851.2:c.180+126A>G	ENSP00000409000.2:n.180+126A>G
ENST00000613087.4:c.192+126A>G	ENSP00000481633.1:n.192+126A>G
NM_172139.2:c.180+126A>G	NP_742151.2:n.180+126A>G
XM_005258765.3:c.192+126A>G	XP_005258822.1:n.192+126A>G
XM_011526757.1:c.192+126A>G	XP_011525059.1:n.192+126A>G
NM_001346937.1:c.192+126A>G	NP_001333866.1:n.192+126A>G
NM_172139.3:c.180+126A>G	NP_742151.2:n.180+126A>G
NM_172139.4:c.180+126A>G MANE Select	NP_742151.2:n.180+126A>G
NM_001346937.2:c.192+126A>G	NP_001333866.1:n.192+126A>G