Canonical Allele Identifier: CA405756086

Gene: IFNL4

Linked Data

• dbSNP Id: rs1600455969
• gnomAD v4: 19-39247736-G-C
• MyVariant Identifiers: chr19:g.39738376G>C (hg19) ; chr19:g.39247736G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247736G>C , CM000681.2:g.39247736G>C	GRCh38
NC_000019.9:g.39738376G>C , CM000681.1:g.39738376G>C	GRCh37
NC_000019.8:g.44430216G>C	NCBI36
NG_042193.1:g.2236C>G
NG_055295.1:g.6121C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.339C>G	ENSP00000476098.1:p.Gly113=
ENST00000610963.1:c.338C>G	ENSP00000481371.1:p.Ala113Gly
ENST00000616270.4:c.224-70C>G	ENSP00000480679.1:n.224-70C>G
ENST00000634680.1:c.152-273C>G	ENSP00000489240.1:n.152-273C>G
ENST00000634967.1:c.223+188C>G	ENSP00000489559.1:n.223+188C>G
NR_074079.1:n.616C>G