Canonical Allele Identifier: CA633069183

Gene: IFNL3

Linked Data

• dbSNP Id: rs1271991325
• gnomAD v2: 19-39735173-G-A
• gnomAD v4: 19-39244533-G-A
• MyVariant Identifiers: chr19:g.39735173G>A (hg19) ; chr19:g.39244533G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244533G>A , CM000681.2:g.39244533G>A	GRCh38
NC_000019.9:g.39735173G>A , CM000681.1:g.39735173G>A	GRCh37
NC_000019.8:g.44427013G>A	NCBI36
NG_042193.1:g.5439C>T
NG_055295.1:g.9324C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-39C>T	ENSP00000481633.1:n.193-39C>T
ENST00000413851.3:c.181-39C>T MANE Select	ENSP00000409000.2:n.181-39C>T
ENST00000413851.2:c.181-39C>T	ENSP00000409000.2:n.181-39C>T
ENST00000613087.4:c.193-39C>T	ENSP00000481633.1:n.193-39C>T
NM_172139.2:c.181-39C>T	NP_742151.2:n.181-39C>T
XM_005258765.3:c.193-39C>T	XP_005258822.1:n.193-39C>T
XM_011526757.1:c.193-39C>T	XP_011525059.1:n.193-39C>T
NM_001346937.1:c.193-39C>T	NP_001333866.1:n.193-39C>T
NM_172139.3:c.181-39C>T	NP_742151.2:n.181-39C>T
NM_172139.4:c.181-39C>T MANE Select	NP_742151.2:n.181-39C>T
NM_001346937.2:c.193-39C>T	NP_001333866.1:n.193-39C>T