Canonical Allele Identifier: CA308219471

Gene: IFNL3

Linked Data

• dbSNP Id: rs75964389
• MyVariant Identifiers: chr19:g.39734971A>G (hg19) ; chr19:g.39244331A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244331A>G , CM000681.2:g.39244331A>G	GRCh38
NC_000019.9:g.39734971A>G , CM000681.1:g.39734971A>G	GRCh37
NC_000019.8:g.44426811A>G	NCBI36
NG_042193.1:g.5641T>C
NG_055295.1:g.9526T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.270+86T>C	ENSP00000481633.1:n.270+86T>C
ENST00000413851.3:c.258+86T>C MANE Select	ENSP00000409000.2:n.258+86T>C
ENST00000413851.2:c.258+86T>C	ENSP00000409000.2:n.258+86T>C
ENST00000613087.4:c.270+86T>C	ENSP00000481633.1:n.270+86T>C
NM_172139.2:c.258+86T>C	NP_742151.2:n.258+86T>C
XM_005258765.3:c.270+86T>C	XP_005258822.1:n.270+86T>C
XM_011526757.1:c.270+86T>C	XP_011525059.1:n.270+86T>C
NM_001346937.1:c.270+86T>C	NP_001333866.1:n.270+86T>C
NM_172139.3:c.258+86T>C	NP_742151.2:n.258+86T>C
NM_172139.4:c.258+86T>C MANE Select	NP_742151.2:n.258+86T>C
NM_001346937.2:c.270+86T>C	NP_001333866.1:n.270+86T>C