Canonical Allele Identifier: CA405752103
Community Standard Title: NM_172139.4(IFNL3):c.542T>G (p.Leu181Arg)
Gene: IFNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243681A>C , CM000681.2:g.39243681A>C GRCh38
NC_000019.9:g.39734321A>C , CM000681.1:g.39734321A>C GRCh37
NC_000019.8:g.44426161A>C NCBI36
NG_042193.1:g.6291T>G

Transcript Alleles

HGVS Amino-acid Change
NM_172139.4:c.542T>G MANE Select NP_742151.2:p.Leu181Arg
ENST00000413851.3:c.542T>G MANE Select ENSP00000409000.2:p.Leu181Arg
NM_001346937.1:c.554T>G NP_001333866.1:p.Leu185Arg
NM_001346937.2:c.554T>G NP_001333866.1:p.Leu185Arg
NM_172139.2:c.542T>G NP_742151.2:p.Leu181Arg
NM_172139.3:c.542T>G NP_742151.2:p.Leu181Arg
ENST00000413851.2:c.542T>G ENSP00000409000.2:p.Leu181Arg
ENST00000613087.4:c.554T>G ENSP00000481633.1:p.Leu185Arg
ENST00000613087.5:c.554T>G ENSP00000481633.1:p.Leu185Arg
XM_005258765.3:c.554T>G XP_005258822.1:p.Leu185Arg
XM_011526757.1:c.554T>G XP_011525059.1:p.Leu185Arg