Canonical Allele Identifier: CA14642620

Gene: IFNL3

Linked Data

• dbSNP Id: rs4803217
• gnomAD v2: 19-39734220-C-A
• gnomAD v3: 19-39243580-C-A
• gnomAD v4: 19-39243580-C-A
• MyVariant Identifiers: chr19:g.39734220C>A (hg19) ; chr19:g.39243580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243580C>A , CM000681.2:g.39243580C>A	GRCh38
NC_000019.9:g.39734220C>A , CM000681.1:g.39734220C>A	GRCh37
NC_000019.8:g.44426060C>A	NCBI36
NG_042193.1:g.6392G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000613087.5:c.*52G>T	ENSP00000481633.1:n.*52G>T
ENST00000413851.3:c.*52G>T MANE Select	ENSP00000409000.2:n.*52G>T
ENST00000613087.4:c.*52G>T	ENSP00000481633.1:n.*52G>T
NM_172139.4:c.*52G>T MANE Select	NP_742151.2:n.*52G>T
NM_001346937.2:c.*52G>T	NP_001333866.1:n.*52G>T