Canonical Allele Identifier: CA405753091

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39735115T>A (hg19) ; chr19:g.39244475T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244475T>A , CM000681.2:g.39244475T>A	GRCh38
NC_000019.9:g.39735115T>A , CM000681.1:g.39735115T>A	GRCh37
NC_000019.8:g.44426955T>A	NCBI36
NG_042193.1:g.5497A>T
NG_055295.1:g.9382A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.212A>T	ENSP00000481633.1:p.Lys71Met
ENST00000413851.3:c.200A>T MANE Select	ENSP00000409000.2:p.Lys67Met
ENST00000413851.2:c.200A>T	ENSP00000409000.2:p.Lys67Met
ENST00000613087.4:c.212A>T	ENSP00000481633.1:p.Lys71Met
NM_172139.2:c.200A>T	NP_742151.2:p.Lys67Met
XM_005258765.3:c.212A>T	XP_005258822.1:p.Lys71Met
XM_011526757.1:c.212A>T	XP_011525059.1:p.Lys71Met
NM_001346937.1:c.212A>T	NP_001333866.1:p.Lys71Met
NM_172139.3:c.200A>T	NP_742151.2:p.Lys67Met
NM_172139.4:c.200A>T MANE Select	NP_742151.2:p.Lys67Met
NM_001346937.2:c.212A>T	NP_001333866.1:p.Lys71Met