Canonical Allele Identifier: CA349002652
Gene: IFIH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.163138882A>T (hg19) chr2:g.162282372A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282372A>T , CM000664.2:g.162282372A>T GRCh38
NC_000002.11:g.163138882A>T , CM000664.1:g.163138882A>T GRCh37
NC_000002.10:g.162847128A>T NCBI36
NG_011495.1:g.41158T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*897T>A ENSP00000513228.1:n.*897T>A
ENST00000648433.1:c.1300T>A ENSP00000496816.1:p.Leu434Met
ENST00000649554.1:n.910T>A
ENST00000649979.2:c.1300T>A MANE Select ENSP00000497271.1:p.Leu434Met
ENST00000679938.1:c.988T>A ENSP00000505518.1:p.Leu330Met
ENST00000263642.2:c.1300T>A ENSP00000263642.2:p.Leu434Met
NM_022168.3:c.1300T>A NP_071451.2:p.Leu434Met
XM_011511628.1:c.583T>A XP_011509930.1:p.Leu195Met
XM_011511629.1:c.1300T>A XP_011509931.1:p.Leu434Met
NM_022168.4:c.1300T>A MANE Select NP_071451.2:p.Leu434Met
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