Canonical Allele Identifier: CA882116918

Gene: IFNL3

Linked Data

• dbSNP Id: rs199508153
• gnomAD v3: 19-39244530-G-A
• gnomAD v4: 19-39244530-G-A
• MyVariant Identifiers: chr19:g.39735170G>A (hg19) ; chr19:g.39244530G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244530G>A , CM000681.2:g.39244530G>A	GRCh38
NC_000019.9:g.39735170G>A , CM000681.1:g.39735170G>A	GRCh37
NC_000019.8:g.44427010G>A	NCBI36
NG_042193.1:g.5442C>T
NG_055295.1:g.9327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-36C>T	ENSP00000481633.1:n.193-36C>T
ENST00000413851.3:c.181-36C>T MANE Select	ENSP00000409000.2:n.181-36C>T
ENST00000413851.2:c.181-36C>T	ENSP00000409000.2:n.181-36C>T
ENST00000613087.4:c.193-36C>T	ENSP00000481633.1:n.193-36C>T
NM_172139.2:c.181-36C>T	NP_742151.2:n.181-36C>T
XM_005258765.3:c.193-36C>T	XP_005258822.1:n.193-36C>T
XM_011526757.1:c.193-36C>T	XP_011525059.1:n.193-36C>T
NM_001346937.1:c.193-36C>T	NP_001333866.1:n.193-36C>T
NM_172139.3:c.181-36C>T	NP_742151.2:n.181-36C>T
NM_172139.4:c.181-36C>T MANE Select	NP_742151.2:n.181-36C>T
NM_001346937.2:c.193-36C>T	NP_001333866.1:n.193-36C>T