gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.59514394 (AFR)
Genomes Max Group AF
0.59398504 (AFR)
Exomes Max Group AF
0.59133029 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.103545430C>A , CM000669.2:g.103545430C>A | GRCh38 |
| NC_000007.13:g.103185877C>A , CM000669.1:g.103185877C>A | GRCh37 |
| NC_000007.12:g.102973113C>A | NCBI36 |
| NG_011877.1:g.449087G>T | |
| NG_011877.2:g.449087G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000424685.3:c.6303-86G>T | ENSP00000388446.3:n.6303-86G>T | |
| ENST00000428762.6:c.6303-86G>T MANE Select | ENSP00000392423.1:n.6303-86G>T | |
| ENST00000679867.1:n.6187-86G>T | ||
| ENST00000679952.1:n.95-86G>T | ||
| ENST00000681034.1:c.6303-86G>T | ENSP00000506075.1:n.6303-86G>T | |
| ENST00000681199.1:n.2071-86G>T | ||
| ENST00000343529.9:c.6303-86G>T | ENSP00000345694.5:n.6303-86G>T | |
| ENST00000424685.2:c.6303-86G>T | ENSP00000388446.2:n.6303-86G>T | |
| ENST00000428762.5:c.6303-86G>T | ENSP00000392423.1:n.6303-86G>T | |
| NM_005045.3:c.6303-86G>T | NP_005036.2:n.6303-86G>T | |
| NM_173054.2:c.6303-86G>T | NP_774959.1:n.6303-86G>T | |
| NM_005045.4:c.6303-86G>T MANE Select | NP_005036.2:n.6303-86G>T | |
| NM_173054.3:c.6303-86G>T | NP_774959.1:n.6303-86G>T |