Canonical Allele Identifier: CA405756507

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247842-G-C
• MyVariant Identifiers: chr19:g.39738482G>C (hg19) ; chr19:g.39247842G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247842G>C , CM000681.2:g.39247842G>C	GRCh38
NC_000019.9:g.39738482G>C , CM000681.1:g.39738482G>C	GRCh37
NC_000019.8:g.44430322G>C	NCBI36
NG_042193.1:g.2130C>G
NG_055295.1:g.6015C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.233C>G	ENSP00000476098.1:p.Ser78Trp
ENST00000610963.1:c.232C>G	ENSP00000481371.1:p.Arg78Gly
ENST00000616270.4:c.223+82C>G	ENSP00000480679.1:n.223+82C>G
ENST00000634680.1:c.152-379C>G	ENSP00000489240.1:n.152-379C>G
ENST00000634967.1:c.223+82C>G	ENSP00000489559.1:n.223+82C>G
NR_074079.1:n.510C>G