Canonical Allele Identifier: CA348990478

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124609G>C (hg19) ; chr2:g.162268099G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162268099G>C , CM000664.2:g.162268099G>C	GRCh38
NC_000002.11:g.163124609G>C , CM000664.1:g.163124609G>C	GRCh37
NC_000002.10:g.162832855G>C	NCBI36
NG_011495.1:g.55431C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*2392C>G	ENSP00000513228.1:n.*2392C>G
ENST00000648433.1:c.2678C>G	ENSP00000496816.1:p.Thr893Ser
ENST00000649426.1:n.39C>G
ENST00000649554.1:n.2405C>G
ENST00000649979.2:c.2795C>G MANE Select	ENSP00000497271.1:p.Thr932Ser
ENST00000679938.1:c.2483C>G	ENSP00000505518.1:p.Thr828Ser
ENST00000263642.2:c.2795C>G	ENSP00000263642.2:p.Thr932Ser
NM_022168.3:c.2795C>G	NP_071451.2:p.Thr932Ser
XM_011511628.1:c.2078C>G	XP_011509930.1:p.Thr693Ser
NM_022168.4:c.2795C>G MANE Select	NP_071451.2:p.Thr932Ser