Canonical Allele Identifier: CA405756831

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247971-G-A
• MyVariant Identifiers: chr19:g.39738611G>A (hg19) ; chr19:g.39247971G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247971G>A , CM000681.2:g.39247971G>A	GRCh38
NC_000019.9:g.39738611G>A , CM000681.1:g.39738611G>A	GRCh37
NC_000019.8:g.44430451G>A	NCBI36
NG_042193.1:g.2001C>T
NG_055295.1:g.5886C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.176C>T	ENSP00000476098.1:p.Ala59Val
ENST00000610963.1:c.175C>T	ENSP00000481371.1:p.Gln59Ter
ENST00000616270.4:c.176C>T	ENSP00000480679.1:p.Ala59Val
ENST00000634680.1:c.151+458C>T	ENSP00000489240.1:n.151+458C>T
ENST00000634967.1:c.176C>T	ENSP00000489559.1:p.Ala59Val
NR_074079.1:n.453C>T