Canonical Allele Identifier: CA759851983

Gene: IFIH1

Linked Data

• dbSNP Id: rs1196176190
• gnomAD v3: 2-162275747-T-C
• gnomAD v4: 2-162275747-T-C
• MyVariant Identifiers: chr2:g.163132257T>C (hg19) ; chr2:g.162275747T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162275747T>C , CM000664.2:g.162275747T>C	GRCh38
NC_000002.11:g.163132257T>C , CM000664.1:g.163132257T>C	GRCh37
NC_000002.10:g.162840503T>C	NCBI36
NG_011495.1:g.47783A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*1901+940A>G	ENSP00000513228.1:n.*1901+940A>G
ENST00000648433.1:c.2187+940A>G	ENSP00000496816.1:n.2187+940A>G
ENST00000649554.1:n.1914+940A>G
ENST00000649979.2:c.2304+940A>G MANE Select	ENSP00000497271.1:n.2304+940A>G
ENST00000679938.1:c.1992+940A>G	ENSP00000505518.1:n.1992+940A>G
ENST00000263642.2:c.2304+940A>G	ENSP00000263642.2:n.2304+940A>G
NM_022168.3:c.2304+940A>G	NP_071451.2:n.2304+940A>G
XM_011511628.1:c.1587+940A>G	XP_011509930.1:n.1587+940A>G
NM_022168.4:c.2304+940A>G MANE Select	NP_071451.2:n.2304+940A>G