Canonical Allele Identifier: CA9426049

Gene: IFNL3

Linked Data

• dbSNP Id: rs200225591
• ExAC: 19:39735126 C / T
• gnomAD v2: 19-39735126-C-T
• gnomAD v3: 19-39244486-C-T
• gnomAD v4: 19-39244486-C-T
• MyVariant Identifiers: chr19:g.39735126C>T (hg19) ; chr19:g.39244486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244486C>T , CM000681.2:g.39244486C>T	GRCh38
NC_000019.9:g.39735126C>T , CM000681.1:g.39735126C>T	GRCh37
NC_000019.8:g.44426966C>T	NCBI36
NG_042193.1:g.5486G>A
NG_055295.1:g.9371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.201G>A	ENSP00000481633.1:p.Ser67=
ENST00000413851.3:c.189G>A MANE Select	ENSP00000409000.2:p.Ser63=
ENST00000413851.2:c.189G>A	ENSP00000409000.2:p.Ser63=
ENST00000613087.4:c.201G>A	ENSP00000481633.1:p.Ser67=
NM_172139.2:c.189G>A	NP_742151.2:p.Ser63=
XM_005258765.3:c.201G>A	XP_005258822.1:p.Ser67=
XM_011526757.1:c.201G>A	XP_011525059.1:p.Ser67=
NM_001346937.1:c.201G>A	NP_001333866.1:p.Ser67=
NM_172139.3:c.189G>A	NP_742151.2:p.Ser63=
NM_172139.4:c.189G>A MANE Select	NP_742151.2:p.Ser63=
NM_001346937.2:c.201G>A	NP_001333866.1:p.Ser67=