Canonical Allele Identifier: CA405756628

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247934-G-C
• MyVariant Identifiers: chr19:g.39738574G>C (hg19) ; chr19:g.39247934G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247934G>C , CM000681.2:g.39247934G>C	GRCh38
NC_000019.9:g.39738574G>C , CM000681.1:g.39738574G>C	GRCh37
NC_000019.8:g.44430414G>C	NCBI36
NG_042193.1:g.2038C>G
NG_055295.1:g.5923C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.213C>G	ENSP00000476098.1:p.Ser71=
ENST00000610963.1:c.212C>G	ENSP00000481371.1:p.Pro71Arg
ENST00000616270.4:c.213C>G	ENSP00000480679.1:p.Ser71=
ENST00000634680.1:c.152-471C>G	ENSP00000489240.1:n.152-471C>G
ENST00000634967.1:c.213C>G	ENSP00000489559.1:p.Ser71=
NR_074079.1:n.490C>G