Canonical Allele Identifier: CA429528268

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124064T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162267554T>C , CM000664.2:g.162267554T>C	GRCh38
NC_000002.11:g.163124064T>C , CM000664.1:g.163124064T>C	GRCh37
NC_000002.10:g.162832310T>C	NCBI36
NG_011495.1:g.55976A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*2420A>G	ENSP00000513228.1:n.*2420A>G
ENST00000648433.1:c.2706A>G	ENSP00000496816.1:p.Val902=
ENST00000649426.1:n.584A>G
ENST00000649554.1:n.2433A>G
ENST00000649979.2:c.2823A>G MANE Select	ENSP00000497271.1:p.Val941=
ENST00000679938.1:c.2511A>G	ENSP00000505518.1:p.Val837=
ENST00000263642.2:c.2823A>G	ENSP00000263642.2:p.Val941=
NM_022168.3:c.2823A>G	NP_071451.2:p.Val941=
XM_011511628.1:c.2106A>G	XP_011509930.1:p.Val702=
NM_022168.4:c.2823A>G MANE Select	NP_071451.2:p.Val941=