Canonical Allele Identifier: CA349013716

Gene: IFIH1

Linked Data

• dbSNP Id: rs1683541983
• MyVariant Identifiers: chr2:g.163174546G>T (hg19) ; chr2:g.162318036G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162318036G>T , CM000664.2:g.162318036G>T	GRCh38
NC_000002.11:g.163174546G>T , CM000664.1:g.163174546G>T	GRCh37
NC_000002.10:g.162882792G>T	NCBI36
NG_011495.1:g.5494C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.272C>A	ENSP00000513228.1:p.Ala91Asp
ENST00000648433.1:c.272C>A	ENSP00000496816.1:p.Ala91Asp
ENST00000649979.2:c.272C>A MANE Select	ENSP00000497271.1:p.Ala91Asp
ENST00000679938.1:c.107C>A	ENSP00000505518.1:p.Ala36Asp
ENST00000263642.2:c.272C>A	ENSP00000263642.2:p.Ala91Asp
ENST00000421365.2:c.272C>A	ENSP00000408450.2:p.Ala91Asp
NM_022168.3:c.272C>A	NP_071451.2:p.Ala91Asp
XM_011511629.1:c.272C>A	XP_011509931.1:p.Ala91Asp
NM_022168.4:c.272C>A MANE Select	NP_071451.2:p.Ala91Asp