Canonical Allele Identifier: CA2335422200
Gene: IFNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39244675T= , CM000681.2:g.39244675T= GRCh38
NC_000019.9:g.39735315T= , CM000681.1:g.39735315T= GRCh37
NC_000019.8:g.44427155T= NCBI36
NG_042193.1:g.5297A=
NG_055295.1:g.9182A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.192+113A= ENSP00000481633.1:n.192+113A=
ENST00000413851.3:c.180+113A= MANE Select ENSP00000409000.2:n.180+113A=
ENST00000413851.2:c.180+113A= ENSP00000409000.2:n.180+113A=
ENST00000613087.4:c.192+113A= ENSP00000481633.1:n.192+113A=
NM_172139.2:c.180+113A= NP_742151.2:n.180+113A=
XM_005258765.3:c.192+113A= XP_005258822.1:n.192+113A=
XM_011526757.1:c.192+113A= XP_011525059.1:n.192+113A=
NM_001346937.1:c.192+113A= NP_001333866.1:n.192+113A=
NM_172139.3:c.180+113A= NP_742151.2:n.180+113A=
NM_172139.4:c.180+113A= MANE Select NP_742151.2:n.180+113A=
NM_001346937.2:c.192+113A= NP_001333866.1:n.192+113A=