Canonical Allele Identifier: CA349013532

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163174456A>T (hg19) ; chr2:g.162317946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162317946A>T , CM000664.2:g.162317946A>T	GRCh38
NC_000002.11:g.163174456A>T , CM000664.1:g.163174456A>T	GRCh37
NC_000002.10:g.162882702A>T	NCBI36
NG_011495.1:g.5584T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.362T>A	ENSP00000513228.1:p.Leu121His
ENST00000648433.1:c.362T>A	ENSP00000496816.1:p.Leu121His
ENST00000649979.2:c.362T>A MANE Select	ENSP00000497271.1:p.Leu121His
ENST00000679938.1:c.197T>A	ENSP00000505518.1:p.Leu66His
ENST00000263642.2:c.362T>A	ENSP00000263642.2:p.Leu121His
ENST00000421365.2:c.362T>A	ENSP00000408450.2:p.Leu121His
NM_022168.3:c.362T>A	NP_071451.2:p.Leu121His
XM_011511629.1:c.362T>A	XP_011509931.1:p.Leu121His
NM_022168.4:c.362T>A MANE Select	NP_071451.2:p.Leu121His