Canonical Allele Identifier: CA882115790

Gene: IFNL3

Linked Data

• dbSNP Id: rs1488157581
• gnomAD v3: 19-39243613-T-C
• gnomAD v4: 19-39243613-T-C
• MyVariant Identifiers: chr19:g.39734253T>C (hg19) ; chr19:g.39243613T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243613T>C , CM000681.2:g.39243613T>C	GRCh38
NC_000019.9:g.39734253T>C , CM000681.1:g.39734253T>C	GRCh37
NC_000019.8:g.44426093T>C	NCBI36
NG_042193.1:g.6359A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000613087.5:c.*19A>G	ENSP00000481633.1:n.*19A>G
ENST00000413851.3:c.*19A>G MANE Select	ENSP00000409000.2:n.*19A>G
ENST00000413851.2:c.*19A>G	ENSP00000409000.2:n.*19A>G
ENST00000613087.4:c.*19A>G	ENSP00000481633.1:n.*19A>G
XM_005258765.3:c.*19A>G	XP_005258822.1:n.*19A>G
XM_011526757.1:c.*19A>G	XP_011525059.1:n.*19A>G
NM_001346937.1:c.622A>G	NP_001333866.1:n.622A>G
NM_172139.3:c.*19A>G	NP_742151.2:n.*19A>G
NM_172139.4:c.*19A>G MANE Select	NP_742151.2:n.*19A>G
NM_001346937.2:c.*19A>G	NP_001333866.1:n.*19A>G