Canonical Allele Identifier: CA633069174

Gene: IFNL3

Linked Data

• dbSNP Id: rs1434043785
• gnomAD v2: 19-39735102-G-GTCCTTCAGCAGTCCTT
• gnomAD v4: 19-39244462-G-GTCCTTCAGCAGTCCTT
• MyVariant Identifiers: chr19:g.39735102_39735103insTCCTTCAGCAGTCCTT (hg19) ; chr19:g.39244462_39244463insTCCTTCAGCAGTCCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244462_39244463insTCCTTCAGCAGTCCTT , CM000681.2:g.39244462_39244463insTCCTTCAGCAGTCCTT	GRCh38
NC_000019.9:g.39735102_39735103insTCCTTCAGCAGTCCTT , CM000681.1:g.39735102_39735103insTCCTTCAGCAGTCCTT	GRCh37
NC_000019.8:g.44426942_44426943insTCCTTCAGCAGTCCTT	NCBI36
NG_042193.1:g.5509_5510insAAGGACTGCTGAAGGA
NG_055295.1:g.9394_9395insAAGGACTGCTGAAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.224_225insAAGGACTGCTGAAGGA	ENSP00000481633.1:p.Cys75Ter
ENST00000413851.3:c.212_213insAAGGACTGCTGAAGGA MANE Select	ENSP00000409000.2:p.Cys71Ter
ENST00000413851.2:c.212_213insAAGGACTGCTGAAGGA	ENSP00000409000.2:p.Cys71Ter
ENST00000613087.4:c.224_225insAAGGACTGCTGAAGGA	ENSP00000481633.1:p.Cys75Ter
NM_172139.2:c.212_213insAAGGACTGCTGAAGGA	NP_742151.2:p.Cys71Ter
XM_005258765.3:c.224_225insAAGGACTGCTGAAGGA	XP_005258822.1:p.Cys75Ter
XM_011526757.1:c.224_225insAAGGACTGCTGAAGGA	XP_011525059.1:p.Cys75Ter
NM_001346937.1:c.224_225insAAGGACTGCTGAAGGA	NP_001333866.1:p.Cys75Ter
NM_172139.3:c.212_213insAAGGACTGCTGAAGGA	NP_742151.2:p.Cys71Ter
NM_172139.4:c.212_213insAAGGACTGCTGAAGGA MANE Select	NP_742151.2:p.Cys71Ter
NM_001346937.2:c.224_225insAAGGACTGCTGAAGGA	NP_001333866.1:p.Cys75Ter