Canonical Allele Identifier: CA405756206

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074955915
• MyVariant Identifiers: chr19:g.39738407G>A (hg19) ; chr19:g.39247767G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247767G>A , CM000681.2:g.39247767G>A	GRCh38
NC_000019.9:g.39738407G>A , CM000681.1:g.39738407G>A	GRCh37
NC_000019.8:g.44430247G>A	NCBI36
NG_042193.1:g.2205C>T
NG_055295.1:g.6090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.308C>T	ENSP00000476098.1:p.Pro103Leu
ENST00000610963.1:c.307C>T	ENSP00000481371.1:p.Pro103Ser
ENST00000616270.4:c.224-101C>T	ENSP00000480679.1:n.224-101C>T
ENST00000634680.1:c.152-304C>T	ENSP00000489240.1:n.152-304C>T
ENST00000634967.1:c.223+157C>T	ENSP00000489559.1:n.223+157C>T
NR_074079.1:n.585C>T