Canonical Allele Identifier: CA405753088

Gene: IFNL3

Linked Data

• dbSNP Id: rs201153643
• gnomAD v3: 19-39244473-C-G
• gnomAD v4: 19-39244473-C-G
• MyVariant Identifiers: chr19:g.39735113C>G (hg19) ; chr19:g.39244473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244473C>G , CM000681.2:g.39244473C>G	GRCh38
NC_000019.9:g.39735113C>G , CM000681.1:g.39735113C>G	GRCh37
NC_000019.8:g.44426953C>G	NCBI36
NG_042193.1:g.5499G>C
NG_055295.1:g.9384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.214G>C	ENSP00000481633.1:p.Asp72His
ENST00000413851.3:c.202G>C MANE Select	ENSP00000409000.2:p.Asp68His
ENST00000413851.2:c.202G>C	ENSP00000409000.2:p.Asp68His
ENST00000613087.4:c.214G>C	ENSP00000481633.1:p.Asp72His
NM_172139.2:c.202G>C	NP_742151.2:p.Asp68His
XM_005258765.3:c.214G>C	XP_005258822.1:p.Asp72His
XM_011526757.1:c.214G>C	XP_011525059.1:p.Asp72His
NM_001346937.1:c.214G>C	NP_001333866.1:p.Asp72His
NM_172139.3:c.202G>C	NP_742151.2:p.Asp68His
NM_172139.4:c.202G>C MANE Select	NP_742151.2:p.Asp68His
NM_001346937.2:c.214G>C	NP_001333866.1:p.Asp72His