Canonical Allele Identifier: CA9426144

Gene: IFNL4

Linked Data

• dbSNP Id: rs376448576
• ExAC: 19:39738669 A / G
• gnomAD v2: 19-39738669-A-G
• gnomAD v3: 19-39248029-A-G
• gnomAD v4: 19-39248029-A-G
• MyVariant Identifiers: chr19:g.39738669A>G (hg19) ; chr19:g.39248029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39248029A>G , CM000681.2:g.39248029A>G	GRCh38
NC_000019.9:g.39738669A>G , CM000681.1:g.39738669A>G	GRCh37
NC_000019.8:g.44430509A>G	NCBI36
NG_042193.1:g.1943T>C
NG_055295.1:g.5828T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.152-34T>C	ENSP00000476098.1:n.152-34T>C
ENST00000610963.1:c.151-34T>C	ENSP00000481371.1:n.151-34T>C
ENST00000616270.4:c.152-34T>C	ENSP00000480679.1:n.152-34T>C
ENST00000634680.1:c.151+400T>C	ENSP00000489240.1:n.151+400T>C
ENST00000634967.1:c.152-34T>C	ENSP00000489559.1:n.152-34T>C
NR_074079.1:n.429-34T>C