Canonical Allele Identifier: CA9426017

Gene: IFNL3

Linked Data

• dbSNP Id: rs773737295
• ExAC: 19:39735015 C / T
• gnomAD v2: 19-39735015-C-T
• gnomAD v3: 19-39244375-C-T
• gnomAD v4: 19-39244375-C-T
• MyVariant Identifiers: chr19:g.39735015C>T (hg19) ; chr19:g.39244375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244375C>T , CM000681.2:g.39244375C>T	GRCh38
NC_000019.9:g.39735015C>T , CM000681.1:g.39735015C>T	GRCh37
NC_000019.8:g.44426855C>T	NCBI36
NG_042193.1:g.5597G>A
NG_055295.1:g.9482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.270+42G>A	ENSP00000481633.1:n.270+42G>A
ENST00000413851.3:c.258+42G>A MANE Select	ENSP00000409000.2:n.258+42G>A
ENST00000413851.2:c.258+42G>A	ENSP00000409000.2:n.258+42G>A
ENST00000613087.4:c.270+42G>A	ENSP00000481633.1:n.270+42G>A
NM_172139.2:c.258+42G>A	NP_742151.2:n.258+42G>A
XM_005258765.3:c.270+42G>A	XP_005258822.1:n.270+42G>A
XM_011526757.1:c.270+42G>A	XP_011525059.1:n.270+42G>A
NM_001346937.1:c.270+42G>A	NP_001333866.1:n.270+42G>A
NM_172139.3:c.258+42G>A	NP_742151.2:n.258+42G>A
NM_172139.4:c.258+42G>A MANE Select	NP_742151.2:n.258+42G>A
NM_001346937.2:c.270+42G>A	NP_001333866.1:n.270+42G>A