Canonical Allele Identifier: CA405753092
Gene: IFNL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39244475T>C , CM000681.2:g.39244475T>C GRCh38
NC_000019.9:g.39735115T>C , CM000681.1:g.39735115T>C GRCh37
NC_000019.8:g.44426955T>C NCBI36
NG_042193.1:g.5497A>G
NG_055295.1:g.9382A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.212A>G ENSP00000481633.1:p.Lys71Arg
ENST00000413851.3:c.200A>G MANE Select ENSP00000409000.2:p.Lys67Arg
ENST00000413851.2:c.200A>G ENSP00000409000.2:p.Lys67Arg
ENST00000613087.4:c.212A>G ENSP00000481633.1:p.Lys71Arg
NM_172139.2:c.200A>G NP_742151.2:p.Lys67Arg
XM_005258765.3:c.212A>G XP_005258822.1:p.Lys71Arg
XM_011526757.1:c.212A>G XP_011525059.1:p.Lys71Arg
NM_001346937.1:c.212A>G NP_001333866.1:p.Lys71Arg
NM_172139.3:c.200A>G NP_742151.2:p.Lys67Arg
NM_172139.4:c.200A>G MANE Select NP_742151.2:p.Lys67Arg
NM_001346937.2:c.212A>G NP_001333866.1:p.Lys71Arg