gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.43744758 (AFR)
Genomes Max Group AF
0.43744758 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.27693337T>C , CM000673.2:g.27693337T>C | GRCh38 |
| NC_000011.9:g.27714884T>C , CM000673.1:g.27714884T>C | GRCh37 |
| NC_000011.8:g.27671460T>C | NCBI36 |
| NG_011794.1:g.33722A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356660.9:c.-22+6827A>G (BDNF) MANE Select | ENSP00000349084.4:n.-22+6827A>G | |
| ENST00000314915.6:c.3+28075A>G (BDNF) | ENSP00000320002.6:n.3+28075A>G | |
| ENST00000356660.8:c.-22+6827A>G (BDNF) | ENSP00000349084.4:n.-22+6827A>G | |
| ENST00000395978.7:c.-22+27092A>G (BDNF) | ENSP00000379302.3:n.-22+27092A>G | |
| ENST00000395980.6:c.-22+7960A>G (BDNF) | ENSP00000379304.2:n.-22+7960A>G | |
| ENST00000395981.7:c.-22+27009A>G (BDNF) | ENSP00000379305.3:n.-22+27009A>G | |
| ENST00000395983.7:c.-22+7634A>G (BDNF) | ENSP00000379307.3:n.-22+7634A>G | |
| ENST00000395986.6:c.24+6045A>G (BDNF) | ENSP00000379309.2:n.24+6045A>G | |
| ENST00000418212.5:c.-129+6827A>G (BDNF) | ENSP00000400502.1:n.-129+6827A>G | |
| ENST00000420794.2:c.-422+7634A>G (BDNF) | ENSP00000389564.1:n.-422+7634A>G | |
| ENST00000438929.5:c.-59+7634A>G (BDNF) | ENSP00000414303.1:n.-59+7634A>G | |
| ENST00000525950.5:c.-22+27307A>G (BDNF) | ENSP00000432035.1:n.-22+27307A>G | |
| ENST00000530786.5:c.-59+7634A>G (BDNF) | ENSP00000433003.1:n.-59+7634A>G | |
| ENST00000530861.5:c.-22+7339A>G (BDNF) | ENSP00000435564.1:n.-22+7339A>G | |
| ENST00000532997.5:c.-22+26174A>G (BDNF) | ENSP00000435805.1:n.-22+26174A>G | |
| ENST00000533131.5:c.-22+6146A>G (BDNF) | ENSP00000432727.1:n.-22+6146A>G | |
| ENST00000533246.5:c.-22+6845A>G (BDNF) | ENSP00000432376.1:n.-22+6845A>G | |
| ENST00000584049.5:n.337+7960A>G (BDNF) | ||
| NM_001143805.1:c.-22+27307A>G (BDNF) | NP_001137277.1:n.-22+27307A>G | |
| NM_001143806.1:c.-22+27092A>G (BDNF) | NP_001137278.1:n.-22+27092A>G | |
| NM_001143807.1:c.-22+26174A>G (BDNF) | NP_001137279.1:n.-22+26174A>G | |
| NM_001143808.1:c.-22+7644A>G (BDNF) | NP_001137280.1:n.-22+7644A>G | |
| NM_001143809.1:c.66+7634A>G (BDNF) | NP_001137281.1:n.66+7634A>G | |
| NM_001143810.1:c.-59+7634A>G (BDNF) | NP_001137282.1:n.-59+7634A>G | |
| NM_001143811.1:c.-422+7634A>G (BDNF) | NP_001137283.1:n.-422+7634A>G | |
| NM_001143812.1:c.-22+7339A>G (BDNF) | NP_001137284.1:n.-22+7339A>G | |
| NM_001143813.1:c.-22+6845A>G (BDNF) | NP_001137285.1:n.-22+6845A>G | |
| NM_001143814.1:c.-129+6827A>G (BDNF) | NP_001137286.1:n.-129+6827A>G | |
| NM_001709.4:c.-22+6827A>G (BDNF) | NP_001700.2:n.-22+6827A>G | |
| NM_170731.4:c.3+28075A>G (BDNF) | NP_733927.1:n.3+28075A>G | |
| NM_170732.4:c.-22+27009A>G (BDNF) | NP_733928.1:n.-22+27009A>G | |
| NM_170733.3:c.-22+7960A>G (BDNF) | NP_733929.1:n.-22+7960A>G | |
| NM_170734.3:c.24+6045A>G (BDNF) | NP_733930.1:n.24+6045A>G | |
| NR_033312.1:n.1342+2197T>C (BDNF-AS) | ||
| NR_033313.1:n.586-4141T>C (BDNF-AS) | ||
| NR_033315.1:n.744-4141T>C (BDNF-AS) | ||
| NM_001709.5:c.-22+6827A>G (BDNF) MANE Select | NP_001700.2:n.-22+6827A>G | |
| NM_001143807.2:c.-22+26174A>G (BDNF) | NP_001137279.1:n.-22+26174A>G | |
| NM_001143813.2:c.-22+6845A>G (BDNF) | NP_001137285.1:n.-22+6845A>G | |
| NM_001143814.2:c.-129+6827A>G (BDNF) | NP_001137286.1:n.-129+6827A>G | |
| NM_170731.5:c.3+28075A>G (BDNF) | NP_733927.1:n.3+28075A>G | |
| NM_001143808.2:c.-22+7644A>G (BDNF) | NP_001137280.1:n.-22+7644A>G | |
| NM_001143809.2:c.66+7634A>G (BDNF) | NP_001137281.1:n.66+7634A>G | |
| NM_001143810.2:c.-59+7634A>G (BDNF) | NP_001137282.1:n.-59+7634A>G | |
| NM_001143811.2:c.-422+7634A>G (BDNF) | NP_001137283.1:n.-422+7634A>G | |
| NM_001143812.2:c.-22+7339A>G (BDNF) | NP_001137284.1:n.-22+7339A>G | |
| NM_170733.4:c.-22+7960A>G (BDNF) | NP_733929.1:n.-22+7960A>G | |
| NM_170734.4:c.24+6045A>G (BDNF) | NP_733930.1:n.24+6045A>G |