Canonical Allele Identifier: CA10147400
Gene: MIF HGNC NCBI
MIF-AS1 HGNC NCBI
ClinVar RCV:
RCV003912215
ClinVar Variation:
3035802
dbSNP:
754953765
gnomAD v2:
22:24237054 C / A
gnomAD v3:
22:23894867 C / A
gnomAD v4:
chr22-23894867-C-A
Joint Max Group AF 0.0009359 (AMR)
Genomes Max Group AF 0.0016358 (AMR)
Exomes Max Group AF 0.0005178 (AMR)
MyVariant.info:
GRCh38 chr22:g.23894867C>A
GRCh37 chr22:g.24237054C>A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23894867C>A , CM000684.2:g.23894867C>A GRCh38
NC_000022.10:g.24237054C>A , CM000684.1:g.24237054C>A GRCh37
NC_000022.9:g.22567054C>A NCBI36
NG_012099.1:g.5490C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215754.8:c.204C>A (MIF) MANE Select ENSP00000215754.7:p.Ile68=
ENST00000215754.7:c.204C>A (MIF) ENSP00000215754.7:p.Ile68=
ENST00000433835.3:c.527C>A ENSP00000400325.3:p.Ser176Ter
ENST00000465752.1:n.229C>A (MIF)
ENST00000498385.1:n.170C>A (MIF)
NM_002415.1:c.204C>A (MIF) NP_002406.1:p.Ile68=
NR_038911.1:n.1035G>T (MIF-AS1)
NM_002415.2:c.204C>A (MIF) MANE Select NP_002406.1:p.Ile68=
Search 100 bp 5'
Search 100 bp 3'