Canonical Allele Identifier: CA308189430

Gene: IFNL4

Linked Data

• dbSNP Id: rs968700124
• gnomAD v2: 19-39738550-C-A
• gnomAD v3: 19-39247910-C-A
• gnomAD v4: 19-39247910-C-A
• MyVariant Identifiers: chr19:g.39738550C>A (hg19) ; chr19:g.39247910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247910C>A , CM000681.2:g.39247910C>A	GRCh38
NC_000019.9:g.39738550C>A , CM000681.1:g.39738550C>A	GRCh37
NC_000019.8:g.44430390C>A	NCBI36
NG_042193.1:g.2062G>T
NG_055295.1:g.5947G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.223+14G>T	ENSP00000476098.1:n.223+14G>T
ENST00000610963.1:c.222+14G>T	ENSP00000481371.1:n.222+14G>T
ENST00000616270.4:c.223+14G>T	ENSP00000480679.1:n.223+14G>T
ENST00000634680.1:c.152-447G>T	ENSP00000489240.1:n.152-447G>T
ENST00000634967.1:c.223+14G>T	ENSP00000489559.1:n.223+14G>T
NR_074079.1:n.500+14G>T