Canonical Allele Identifier: CA349002477

Gene: IFIH1

Linked Data

• gnomAD v4: 2-162281480-T-C
• MyVariant Identifiers: chr2:g.163137990T>C (hg19) ; chr2:g.162281480T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162281480T>C , CM000664.2:g.162281480T>C	GRCh38
NC_000002.11:g.163137990T>C , CM000664.1:g.163137990T>C	GRCh37
NC_000002.10:g.162846236T>C	NCBI36
NG_011495.1:g.42050A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*969A>G	ENSP00000513228.1:n.*969A>G
ENST00000648433.1:c.1372A>G	ENSP00000496816.1:p.Met458Val
ENST00000649554.1:n.982A>G
ENST00000649979.2:c.1372A>G MANE Select	ENSP00000497271.1:p.Met458Val
ENST00000679938.1:c.1060A>G	ENSP00000505518.1:p.Met354Val
ENST00000263642.2:c.1372A>G	ENSP00000263642.2:p.Met458Val
NM_022168.3:c.1372A>G	NP_071451.2:p.Met458Val
XM_011511628.1:c.655A>G	XP_011509930.1:p.Met219Val
XM_011511629.1:c.1372A>G	XP_011509931.1:p.Met458Val
NM_022168.4:c.1372A>G MANE Select	NP_071451.2:p.Met458Val