Canonical Allele Identifier: CA14922029
Gene: MIF HGNC NCBI
MIF-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.23894205G>C
GRCh37 chr22:g.24236392G>C
gnomAD v2:
22:24236392 G / C
gnomAD v3:
22:23894205 G / C
gnomAD v4:
chr22-23894205-G-C
Joint Max Group AF 0.4041592 (AFR)
Genomes Max Group AF 0.40512148 (AFR)
Exomes Max Group AF 0.3907173 (AFR)
ClinVar RCV:
RCV000015433
ClinVar Variation:
14359
dbSNP:
755622
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23894205G>C , CM000684.2:g.23894205G>C GRCh38
NC_000022.10:g.24236392G>C , CM000684.1:g.24236392G>C GRCh37
NC_000022.9:g.22566392G>C NCBI36
NG_012099.1:g.4828G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215754.7:c.-270G>C (MIF) ENSP00000215754.7:n.-270G>C
ENST00000433835.3:c.432-567G>C ENSP00000400325.3:n.432-567G>C
NR_038911.1:n.1697C>G (MIF-AS1)
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