Canonical Allele Identifier: CA429536015
Gene: IFIH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.163138940A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282430A>T , CM000664.2:g.162282430A>T GRCh38
NC_000002.11:g.163138940A>T , CM000664.1:g.163138940A>T GRCh37
NC_000002.10:g.162847186A>T NCBI36
NG_011495.1:g.41100T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*839T>A ENSP00000513228.1:n.*839T>A
ENST00000648433.1:c.1242T>A ENSP00000496816.1:p.Ala414=
ENST00000649554.1:n.852T>A
ENST00000649979.2:c.1242T>A MANE Select ENSP00000497271.1:p.Ala414=
ENST00000679938.1:c.930T>A ENSP00000505518.1:p.Ala310=
ENST00000263642.2:c.1242T>A ENSP00000263642.2:p.Ala414=
NM_022168.3:c.1242T>A NP_071451.2:p.Ala414=
XM_011511628.1:c.525T>A XP_011509930.1:p.Ala175=
XM_011511629.1:c.1242T>A XP_011509931.1:p.Ala414=
NM_022168.4:c.1242T>A MANE Select NP_071451.2:p.Ala414=