Canonical Allele Identifier: CA405755034

Gene: IFNL4

Linked Data

• dbSNP Id: rs1568553961
• MyVariant Identifiers: chr19:g.39738098C>A (hg19) ; chr19:g.39247458C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247458C>A , CM000681.2:g.39247458C>A	GRCh38
NC_000019.9:g.39738098C>A , CM000681.1:g.39738098C>A	GRCh37
NC_000019.8:g.44429938C>A	NCBI36
NG_042193.1:g.2514G>T
NG_055295.1:g.6399G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.373G>T	ENSP00000476098.1:p.Ala125Ser
ENST00000610963.1:c.372G>T	ENSP00000481371.1:p.Glu124Asp
ENST00000616270.4:c.422+10G>T	ENSP00000480679.1:n.422+10G>T
ENST00000634680.1:c.157G>T	ENSP00000489240.1:p.Ala53Ser
ENST00000634967.1:c.229G>T	ENSP00000489559.1:p.Ala77Ser
NR_074079.1:n.650G>T