Linked Data
dbSNP Id:
rs2096525
ExAC:
22:24236819 T / C
gnomAD v2:
22-24236819-T-C
gnomAD v3:
22-23894632-T-C
gnomAD v4:
22-23894632-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23894632T>C , CM000684.2:g.23894632T>C | GRCh38 |
| NC_000022.10:g.24236819T>C , CM000684.1:g.24236819T>C | GRCh37 |
| NC_000022.9:g.22566819T>C | NCBI36 |
| NG_012099.1:g.5255T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000215754.8:c.108+50T>C (MIF) MANE Select | ENSP00000215754.7:n.108+50T>C | |
| ENST00000215754.7:c.108+50T>C (MIF) | ENSP00000215754.7:n.108+50T>C | |
| ENST00000433835.3:c.432-140T>C | ENSP00000400325.3:n.432-140T>C | |
| ENST00000465752.1:n.133+50T>C (MIF) | ||
| NM_002415.1:c.108+50T>C (MIF) | NP_002406.1:n.108+50T>C | |
| NR_038911.1:n.1270A>G (MIF-AS1) | ||
| NM_002415.2:c.108+50T>C (MIF) MANE Select | NP_002406.1:n.108+50T>C |