Canonical Allele Identifier: CA429535743
Gene: IFIH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.163137991G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162281481G>A , CM000664.2:g.162281481G>A GRCh38
NC_000002.11:g.163137991G>A , CM000664.1:g.163137991G>A GRCh37
NC_000002.10:g.162846237G>A NCBI36
NG_011495.1:g.42049C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697291.1:c.*968C>T ENSP00000513228.1:n.*968C>T
ENST00000648433.1:c.1371C>T ENSP00000496816.1:p.Ile457=
ENST00000649554.1:n.981C>T
ENST00000649979.2:c.1371C>T MANE Select ENSP00000497271.1:p.Ile457=
ENST00000679938.1:c.1059C>T ENSP00000505518.1:p.Ile353=
ENST00000263642.2:c.1371C>T ENSP00000263642.2:p.Ile457=
NM_022168.3:c.1371C>T NP_071451.2:p.Ile457=
XM_011511628.1:c.654C>T XP_011509930.1:p.Ile218=
XM_011511629.1:c.1371C>T XP_011509931.1:p.Ile457=
NM_022168.4:c.1371C>T MANE Select NP_071451.2:p.Ile457=