Canonical Allele Identifier: CA1934567

Gene: IFIH1

Linked Data

• dbSNP Id: rs766971421
• ExAC: 2:163138850 T / TA
• gnomAD v2: 2-163138850-T-TA
• gnomAD v3: 2-162282340-T-TA
• gnomAD v4: 2-162282340-T-TA
• MyVariant Identifiers: chr2:g.163138850_163138851insA (hg19) ; chr2:g.162282340_162282341insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282340_162282341insA , CM000664.2:g.162282340_162282341insA	GRCh38
NC_000002.11:g.163138850_163138851insA , CM000664.1:g.163138850_163138851insA	GRCh37
NC_000002.10:g.162847096_162847097insA	NCBI36
NG_011495.1:g.41189_41190insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*903+25_*903+26insT	ENSP00000513228.1:n.*903+25_*903+26insT
ENST00000648433.1:c.1306+25_1306+26insT	ENSP00000496816.1:n.1306+25_1306+26insT
ENST00000649554.1:n.916+25_916+26insT
ENST00000649979.2:c.1306+25_1306+26insT MANE Select	ENSP00000497271.1:n.1306+25_1306+26insT
ENST00000679938.1:c.994+25_994+26insT	ENSP00000505518.1:n.994+25_994+26insT
ENST00000263642.2:c.1306+25_1306+26insT	ENSP00000263642.2:n.1306+25_1306+26insT
NM_022168.3:c.1306+25_1306+26insT	NP_071451.2:n.1306+25_1306+26insT
XM_011511628.1:c.589+25_589+26insT	XP_011509930.1:n.589+25_589+26insT
XM_011511629.1:c.1306+25_1306+26insT	XP_011509931.1:n.1306+25_1306+26insT
NM_022168.4:c.1306+25_1306+26insT MANE Select	NP_071451.2:n.1306+25_1306+26insT