Canonical Allele Identifier: CA349002715
Gene: IFIH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.163138911A>G (hg19) chr2:g.162282401A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282401A>G , CM000664.2:g.162282401A>G GRCh38
NC_000002.11:g.163138911A>G , CM000664.1:g.163138911A>G GRCh37
NC_000002.10:g.162847157A>G NCBI36
NG_011495.1:g.41129T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*868T>C ENSP00000513228.1:n.*868T>C
ENST00000648433.1:c.1271T>C ENSP00000496816.1:p.Leu424Ser
ENST00000649554.1:n.881T>C
ENST00000649979.2:c.1271T>C MANE Select ENSP00000497271.1:p.Leu424Ser
ENST00000679938.1:c.959T>C ENSP00000505518.1:p.Leu320Ser
ENST00000263642.2:c.1271T>C ENSP00000263642.2:p.Leu424Ser
NM_022168.3:c.1271T>C NP_071451.2:p.Leu424Ser
XM_011511628.1:c.554T>C XP_011509930.1:p.Leu185Ser
XM_011511629.1:c.1271T>C XP_011509931.1:p.Leu424Ser
NM_022168.4:c.1271T>C MANE Select NP_071451.2:p.Leu424Ser
Search 100 bp 5'
Search 100 bp 3'