ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA405755912
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247658-G-A
MyVariant Identifiers:
chr19:g.39738298G>A (hg19)
chr19:g.39247658G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247658G>A , CM000681.2:g.39247658G>A
GRCh38
NC_000019.9:g.39738298G>A , CM000681.1:g.39738298G>A
GRCh37
NC_000019.8:g.44430138G>A
NCBI36
NG_042193.1:g.2314C>T
NG_055295.1:g.6199C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.367+50C>T
ENSP00000476098.1:n.367+50C>T
ENST00000610963.1:c.366+50C>T
ENSP00000481371.1:n.366+50C>T
ENST00000616270.4:c.232C>T
ENSP00000480679.1:p.His78Tyr
ENST00000634680.1:c.152-195C>T
ENSP00000489240.1:n.152-195C>T
ENST00000634967.1:c.224-195C>T
ENSP00000489559.1:n.224-195C>T
NR_074079.1:n.644+50C>T
Search 100 bp 5'
Search 100 bp 3'