Canonical Allele Identifier: CA507416262

Gene: IFNL3

Linked Data

• MyVariant Identifiers: chr19:g.39735120C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244480C>G , CM000681.2:g.39244480C>G	GRCh38
NC_000019.9:g.39735120C>G , CM000681.1:g.39735120C>G	GRCh37
NC_000019.8:g.44426960C>G	NCBI36
NG_042193.1:g.5492G>C
NG_055295.1:g.9377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.207G>C	ENSP00000481633.1:p.Leu69=
ENST00000413851.3:c.195G>C MANE Select	ENSP00000409000.2:p.Leu65=
ENST00000413851.2:c.195G>C	ENSP00000409000.2:p.Leu65=
ENST00000613087.4:c.207G>C	ENSP00000481633.1:p.Leu69=
NM_172139.2:c.195G>C	NP_742151.2:p.Leu65=
XM_005258765.3:c.207G>C	XP_005258822.1:p.Leu69=
XM_011526757.1:c.207G>C	XP_011525059.1:p.Leu69=
NM_001346937.1:c.207G>C	NP_001333866.1:p.Leu69=
NM_172139.3:c.195G>C	NP_742151.2:p.Leu65=
NM_172139.4:c.195G>C MANE Select	NP_742151.2:p.Leu65=
NM_001346937.2:c.207G>C	NP_001333866.1:p.Leu69=