Canonical Allele Identifier: CA405755526

Gene: IFNL4

Linked Data

• dbSNP Id: rs1600455816
• MyVariant Identifiers: chr19:g.39738208A>C (hg19) ; chr19:g.39247568A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247568A>C , CM000681.2:g.39247568A>C	GRCh38
NC_000019.9:g.39738208A>C , CM000681.1:g.39738208A>C	GRCh37
NC_000019.8:g.44430048A>C	NCBI36
NG_042193.1:g.2404T>G
NG_055295.1:g.6289T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-105T>G	ENSP00000476098.1:n.368-105T>G
ENST00000610963.1:c.367-105T>G	ENSP00000481371.1:n.367-105T>G
ENST00000616270.4:c.322T>G	ENSP00000480679.1:p.Cys108Gly
ENST00000634680.1:c.152-105T>G	ENSP00000489240.1:n.152-105T>G
ENST00000634967.1:c.224-105T>G	ENSP00000489559.1:n.224-105T>G
NR_074079.1:n.645-105T>G