Canonical Allele Identifier: CA405752160

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39243709-C-G
• MyVariant Identifiers: chr19:g.39734349C>G (hg19) ; chr19:g.39243709C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243709C>G , CM000681.2:g.39243709C>G	GRCh38
NC_000019.9:g.39734349C>G , CM000681.1:g.39734349C>G	GRCh37
NC_000019.8:g.44426189C>G	NCBI36
NG_042193.1:g.6263G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.526G>C	ENSP00000481633.1:p.Ala176Pro
ENST00000413851.3:c.514G>C MANE Select	ENSP00000409000.2:p.Ala172Pro
ENST00000413851.2:c.514G>C	ENSP00000409000.2:p.Ala172Pro
ENST00000613087.4:c.526G>C	ENSP00000481633.1:p.Ala176Pro
NM_172139.2:c.514G>C	NP_742151.2:p.Ala172Pro
XM_005258765.3:c.526G>C	XP_005258822.1:p.Ala176Pro
XM_011526757.1:c.526G>C	XP_011525059.1:p.Ala176Pro
NM_001346937.1:c.526G>C	NP_001333866.1:p.Ala176Pro
NM_172139.3:c.514G>C	NP_742151.2:p.Ala172Pro
NM_172139.4:c.514G>C MANE Select	NP_742151.2:p.Ala172Pro
NM_001346937.2:c.526G>C	NP_001333866.1:p.Ala176Pro