Canonical Allele Identifier: CA405753086

Gene: IFNL3

Linked Data

• gnomAD v3: 19-39244472-T-G
• gnomAD v4: 19-39244472-T-G
• MyVariant Identifiers: chr19:g.39735112T>G (hg19) ; chr19:g.39244472T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244472T>G , CM000681.2:g.39244472T>G	GRCh38
NC_000019.9:g.39735112T>G , CM000681.1:g.39735112T>G	GRCh37
NC_000019.8:g.44426952T>G	NCBI36
NG_042193.1:g.5500A>C
NG_055295.1:g.9385A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.215A>C	ENSP00000481633.1:p.Asp72Ala
ENST00000413851.3:c.203A>C MANE Select	ENSP00000409000.2:p.Asp68Ala
ENST00000413851.2:c.203A>C	ENSP00000409000.2:p.Asp68Ala
ENST00000613087.4:c.215A>C	ENSP00000481633.1:p.Asp72Ala
NM_172139.2:c.203A>C	NP_742151.2:p.Asp68Ala
XM_005258765.3:c.215A>C	XP_005258822.1:p.Asp72Ala
XM_011526757.1:c.215A>C	XP_011525059.1:p.Asp72Ala
NM_001346937.1:c.215A>C	NP_001333866.1:p.Asp72Ala
NM_172139.3:c.203A>C	NP_742151.2:p.Asp68Ala
NM_172139.4:c.203A>C MANE Select	NP_742151.2:p.Asp68Ala
NM_001346937.2:c.215A>C	NP_001333866.1:p.Asp72Ala