Canonical Allele Identifier: CA405753076

Gene: IFNL3

Linked Data

• COSMIC: COSM711516
• MyVariant Identifiers: chr19:g.39735108G>C (hg19) ; chr19:g.39244468G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244468G>C , CM000681.2:g.39244468G>C	GRCh38
NC_000019.9:g.39735108G>C , CM000681.1:g.39735108G>C	GRCh37
NC_000019.8:g.44426948G>C	NCBI36
NG_042193.1:g.5504C>G
NG_055295.1:g.9389C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.219C>G	ENSP00000481633.1:p.Cys73Trp
ENST00000413851.3:c.207C>G MANE Select	ENSP00000409000.2:p.Cys69Trp
ENST00000413851.2:c.207C>G	ENSP00000409000.2:p.Cys69Trp
ENST00000613087.4:c.219C>G	ENSP00000481633.1:p.Cys73Trp
NM_172139.2:c.207C>G	NP_742151.2:p.Cys69Trp
XM_005258765.3:c.219C>G	XP_005258822.1:p.Cys73Trp
XM_011526757.1:c.219C>G	XP_011525059.1:p.Cys73Trp
NM_001346937.1:c.219C>G	NP_001333866.1:p.Cys73Trp
NM_172139.3:c.207C>G	NP_742151.2:p.Cys69Trp
NM_172139.4:c.207C>G MANE Select	NP_742151.2:p.Cys69Trp
NM_001346937.2:c.219C>G	NP_001333866.1:p.Cys73Trp