Canonical Allele Identifier: CA507407743

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738483A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247843A>C , CM000681.2:g.39247843A>C	GRCh38
NC_000019.9:g.39738483A>C , CM000681.1:g.39738483A>C	GRCh37
NC_000019.8:g.44430323A>C	NCBI36
NG_042193.1:g.2129T>G
NG_055295.1:g.6014T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.232T>G	ENSP00000476098.1:p.Ser78Ala
ENST00000610963.1:c.231T>G	ENSP00000481371.1:p.Ala77=
ENST00000616270.4:c.223+81T>G	ENSP00000480679.1:n.223+81T>G
ENST00000634680.1:c.152-380T>G	ENSP00000489240.1:n.152-380T>G
ENST00000634967.1:c.223+81T>G	ENSP00000489559.1:n.223+81T>G
NR_074079.1:n.509T>G