Canonical Allele Identifier: CA882116936

Gene: IFNL3

Linked Data

• dbSNP Id: rs1460259701
• MyVariant Identifiers: chr19:g.39735214C>T (hg19) ; chr19:g.39244574C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244574C>T , CM000681.2:g.39244574C>T	GRCh38
NC_000019.9:g.39735214C>T , CM000681.1:g.39735214C>T	GRCh37
NC_000019.8:g.44427054C>T	NCBI36
NG_042193.1:g.5398G>A
NG_055295.1:g.9283G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-80G>A	ENSP00000481633.1:n.193-80G>A
ENST00000413851.3:c.181-80G>A MANE Select	ENSP00000409000.2:n.181-80G>A
ENST00000413851.2:c.181-80G>A	ENSP00000409000.2:n.181-80G>A
ENST00000613087.4:c.193-80G>A	ENSP00000481633.1:n.193-80G>A
NM_172139.2:c.181-80G>A	NP_742151.2:n.181-80G>A
XM_005258765.3:c.193-80G>A	XP_005258822.1:n.193-80G>A
XM_011526757.1:c.193-80G>A	XP_011525059.1:n.193-80G>A
NM_001346937.1:c.193-80G>A	NP_001333866.1:n.193-80G>A
NM_172139.3:c.181-80G>A	NP_742151.2:n.181-80G>A
NM_172139.4:c.181-80G>A MANE Select	NP_742151.2:n.181-80G>A
NM_001346937.2:c.193-80G>A	NP_001333866.1:n.193-80G>A