Canonical Allele Identifier: CA349002743

Gene: IFIH1

Linked Data

• dbSNP Id: rs1682826868
• MyVariant Identifiers: chr2:g.163138924A>C (hg19) ; chr2:g.162282414A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282414A>C , CM000664.2:g.162282414A>C	GRCh38
NC_000002.11:g.163138924A>C , CM000664.1:g.163138924A>C	GRCh37
NC_000002.10:g.162847170A>C	NCBI36
NG_011495.1:g.41116T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*855T>G	ENSP00000513228.1:n.*855T>G
ENST00000648433.1:c.1258T>G	ENSP00000496816.1:p.Ser420Ala
ENST00000649554.1:n.868T>G
ENST00000649979.2:c.1258T>G MANE Select	ENSP00000497271.1:p.Ser420Ala
ENST00000679938.1:c.946T>G	ENSP00000505518.1:p.Ser316Ala
ENST00000263642.2:c.1258T>G	ENSP00000263642.2:p.Ser420Ala
NM_022168.3:c.1258T>G	NP_071451.2:p.Ser420Ala
XM_011511628.1:c.541T>G	XP_011509930.1:p.Ser181Ala
XM_011511629.1:c.1258T>G	XP_011509931.1:p.Ser420Ala
NM_022168.4:c.1258T>G MANE Select	NP_071451.2:p.Ser420Ala