Canonical Allele Identifier: CA633069317

Gene: IFNL4

Linked Data

• dbSNP Id: rs1452359981
• gnomAD v2: 19-39738653-C-G
• gnomAD v3: 19-39248013-C-G
• gnomAD v4: 19-39248013-C-G
• MyVariant Identifiers: chr19:g.39738653C>G (hg19) ; chr19:g.39248013C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39248013C>G , CM000681.2:g.39248013C>G	GRCh38
NC_000019.9:g.39738653C>G , CM000681.1:g.39738653C>G	GRCh37
NC_000019.8:g.44430493C>G	NCBI36
NG_042193.1:g.1959G>C
NG_055295.1:g.5844G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.152-18G>C	ENSP00000476098.1:n.152-18G>C
ENST00000610963.1:c.151-18G>C	ENSP00000481371.1:n.151-18G>C
ENST00000616270.4:c.152-18G>C	ENSP00000480679.1:n.152-18G>C
ENST00000634680.1:c.151+416G>C	ENSP00000489240.1:n.151+416G>C
ENST00000634967.1:c.152-18G>C	ENSP00000489559.1:n.152-18G>C
NR_074079.1:n.429-18G>C