Canonical Allele Identifier: CA633069120
Gene: IFNL3 HGNC NCBI

Linked Data

dbSNP Id: rs1316413146
gnomAD v2: 19-39734221-C-T
MyVariant Identifiers: chr19:g.39734221C>T (hg19) chr19:g.39243581C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243581C>T , CM000681.2:g.39243581C>T GRCh38
NC_000019.9:g.39734221C>T , CM000681.1:g.39734221C>T GRCh37
NC_000019.8:g.44426061C>T NCBI36
NG_042193.1:g.6391G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000613087.5:c.*51G>A ENSP00000481633.1:n.*51G>A
ENST00000413851.3:c.*51G>A MANE Select ENSP00000409000.2:n.*51G>A
ENST00000613087.4:c.*51G>A ENSP00000481633.1:n.*51G>A
NM_172139.4:c.*51G>A MANE Select NP_742151.2:n.*51G>A
NM_001346937.2:c.*51G>A NP_001333866.1:n.*51G>A
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