Canonical Allele Identifier: CA1934588

Gene: IFIH1

Linked Data

• dbSNP Id: rs780469147
• ExAC: 2:163138957 T / C
• gnomAD v2: 2-163138957-T-C
• gnomAD v4: 2-162282447-T-C
• MyVariant Identifiers: chr2:g.163138957T>C (hg19) ; chr2:g.162282447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282447T>C , CM000664.2:g.162282447T>C	GRCh38
NC_000002.11:g.163138957T>C , CM000664.1:g.163138957T>C	GRCh37
NC_000002.10:g.162847203T>C	NCBI36
NG_011495.1:g.41083A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*822A>G	ENSP00000513228.1:n.*822A>G
ENST00000648433.1:c.1225A>G	ENSP00000496816.1:p.Ile409Val
ENST00000649554.1:n.835A>G
ENST00000649979.2:c.1225A>G MANE Select	ENSP00000497271.1:p.Ile409Val
ENST00000679938.1:c.913A>G	ENSP00000505518.1:p.Ile305Val
ENST00000263642.2:c.1225A>G	ENSP00000263642.2:p.Ile409Val
NM_022168.3:c.1225A>G	NP_071451.2:p.Ile409Val
XM_011511628.1:c.508A>G	XP_011509930.1:p.Ile170Val
XM_011511629.1:c.1225A>G	XP_011509931.1:p.Ile409Val
NM_022168.4:c.1225A>G MANE Select	NP_071451.2:p.Ile409Val