Canonical Allele Identifier: CA348989689

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124018T>C (hg19) ; chr2:g.162267508T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162267508T>C , CM000664.2:g.162267508T>C	GRCh38
NC_000002.11:g.163124018T>C , CM000664.1:g.163124018T>C	GRCh37
NC_000002.10:g.162832264T>C	NCBI36
NG_011495.1:g.56022A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*2466A>G	ENSP00000513228.1:n.*2466A>G
ENST00000648433.1:c.2752A>G	ENSP00000496816.1:p.Asn918Asp
ENST00000649426.1:n.630A>G
ENST00000649554.1:n.2479A>G
ENST00000649979.2:c.2869A>G MANE Select	ENSP00000497271.1:p.Asn957Asp
ENST00000679938.1:c.2557A>G	ENSP00000505518.1:p.Asn853Asp
ENST00000263642.2:c.2869A>G	ENSP00000263642.2:p.Asn957Asp
NM_022168.3:c.2869A>G	NP_071451.2:p.Asn957Asp
XM_011511628.1:c.2152A>G	XP_011509930.1:p.Asn718Asp
NM_022168.4:c.2869A>G MANE Select	NP_071451.2:p.Asn957Asp