Canonical Allele Identifier: CA405752052

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39243654-G-T
• MyVariant Identifiers: chr19:g.39734294G>T (hg19) ; chr19:g.39243654G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243654G>T , CM000681.2:g.39243654G>T	GRCh38
NC_000019.9:g.39734294G>T , CM000681.1:g.39734294G>T	GRCh37
NC_000019.8:g.44426134G>T	NCBI36
NG_042193.1:g.6318C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.581C>A	ENSP00000481633.1:p.Ala194Asp
ENST00000413851.3:c.569C>A MANE Select	ENSP00000409000.2:p.Ala190Asp
ENST00000413851.2:c.569C>A	ENSP00000409000.2:p.Ala190Asp
ENST00000613087.4:c.581C>A	ENSP00000481633.1:p.Ala194Asp
NM_172139.2:c.569C>A	NP_742151.2:p.Ala190Asp
XM_005258765.3:c.581C>A	XP_005258822.1:p.Ala194Asp
XM_011526757.1:c.581C>A	XP_011525059.1:p.Ala194Asp
NM_001346937.1:c.581C>A	NP_001333866.1:p.Ala194Asp
NM_172139.3:c.569C>A	NP_742151.2:p.Ala190Asp
NM_172139.4:c.569C>A MANE Select	NP_742151.2:p.Ala190Asp
NM_001346937.2:c.581C>A	NP_001333866.1:p.Ala194Asp