Canonical Allele Identifier: CA59665141

Gene: IFIH1

Linked Data

• dbSNP Id: rs889256826
• gnomAD v3: 2-162281658-C-A
• gnomAD v4: 2-162281658-C-A
• MyVariant Identifiers: chr2:g.163138168C>A (hg19) ; chr2:g.162281658C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162281658C>A , CM000664.2:g.162281658C>A	GRCh38
NC_000002.11:g.163138168C>A , CM000664.1:g.163138168C>A	GRCh37
NC_000002.10:g.162846414C>A	NCBI36
NG_011495.1:g.41872G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*904-113G>T	ENSP00000513228.1:n.*904-113G>T
ENST00000648433.1:c.1307-113G>T	ENSP00000496816.1:n.1307-113G>T
ENST00000649554.1:n.917-113G>T
ENST00000649979.2:c.1307-113G>T MANE Select	ENSP00000497271.1:n.1307-113G>T
ENST00000679938.1:c.995-113G>T	ENSP00000505518.1:n.995-113G>T
ENST00000263642.2:c.1307-113G>T	ENSP00000263642.2:n.1307-113G>T
NM_022168.3:c.1307-113G>T	NP_071451.2:n.1307-113G>T
XM_011511628.1:c.590-113G>T	XP_011509930.1:n.590-113G>T
XM_011511629.1:c.1307-113G>T	XP_011509931.1:n.1307-113G>T
NM_022168.4:c.1307-113G>T MANE Select	NP_071451.2:n.1307-113G>T