Canonical Allele Identifier: CA507655093

Gene: IFNL3

Linked Data

• dbSNP Id: rs2074925223
• gnomAD v4: 19-39243647-C-T
• MyVariant Identifiers: chr19:g.39734287C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243647C>T , CM000681.2:g.39243647C>T	GRCh38
NC_000019.9:g.39734287C>T , CM000681.1:g.39734287C>T	GRCh37
NC_000019.8:g.44426127C>T	NCBI36
NG_042193.1:g.6325G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.588G>A	ENSP00000481633.1:p.Gly196=
ENST00000413851.3:c.576G>A MANE Select	ENSP00000409000.2:p.Gly192=
ENST00000413851.2:c.576G>A	ENSP00000409000.2:p.Gly192=
ENST00000613087.4:c.588G>A	ENSP00000481633.1:p.Gly196=
NM_172139.2:c.576G>A	NP_742151.2:p.Gly192=
XM_005258765.3:c.588G>A	XP_005258822.1:p.Gly196=
XM_011526757.1:c.588G>A	XP_011525059.1:p.Gly196=
NM_001346937.1:c.588G>A	NP_001333866.1:p.Gly196=
NM_172139.3:c.576G>A	NP_742151.2:p.Gly192=
NM_172139.4:c.576G>A MANE Select	NP_742151.2:p.Gly192=
NM_001346937.2:c.588G>A	NP_001333866.1:p.Gly196=