Canonical Allele Identifier: CA349002642

Gene: IFIH1

Linked Data

• gnomAD v4: 2-162282368-G-A
• MyVariant Identifiers: chr2:g.163138878G>A (hg19) ; chr2:g.162282368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282368G>A , CM000664.2:g.162282368G>A	GRCh38
NC_000002.11:g.163138878G>A , CM000664.1:g.163138878G>A	GRCh37
NC_000002.10:g.162847124G>A	NCBI36
NG_011495.1:g.41162C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*901C>T	ENSP00000513228.1:n.*901C>T
ENST00000648433.1:c.1304C>T	ENSP00000496816.1:p.Ser435Leu
ENST00000649554.1:n.914C>T
ENST00000649979.2:c.1304C>T MANE Select	ENSP00000497271.1:p.Ser435Leu
ENST00000679938.1:c.992C>T	ENSP00000505518.1:p.Ser331Leu
ENST00000263642.2:c.1304C>T	ENSP00000263642.2:p.Ser435Leu
NM_022168.3:c.1304C>T	NP_071451.2:p.Ser435Leu
XM_011511628.1:c.587C>T	XP_011509930.1:p.Ser196Leu
XM_011511629.1:c.1304C>T	XP_011509931.1:p.Ser435Leu
NM_022168.4:c.1304C>T MANE Select	NP_071451.2:p.Ser435Leu