Canonical Allele Identifier: CA405756477

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738473G>A (hg19) ; chr19:g.39247833G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247833G>A , CM000681.2:g.39247833G>A	GRCh38
NC_000019.9:g.39738473G>A , CM000681.1:g.39738473G>A	GRCh37
NC_000019.8:g.44430313G>A	NCBI36
NG_042193.1:g.2139C>T
NG_055295.1:g.6024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.242C>T	ENSP00000476098.1:p.Pro81Leu
ENST00000610963.1:c.241C>T	ENSP00000481371.1:p.His81Tyr
ENST00000616270.4:c.223+91C>T	ENSP00000480679.1:n.223+91C>T
ENST00000634680.1:c.152-370C>T	ENSP00000489240.1:n.152-370C>T
ENST00000634967.1:c.223+91C>T	ENSP00000489559.1:n.223+91C>T
NR_074079.1:n.519C>T