gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.19719043 (AFR)
Genomes Max Group AF
0.19719043 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116781491C>T , CM000673.2:g.116781491C>T | GRCh38 |
| NC_000011.9:g.116652207C>T , CM000673.1:g.116652207C>T | GRCh37 |
| NC_000011.8:g.116157417C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227322.8:c.1179+667G>A MANE Select | ENSP00000227322.3:n.1179+667G>A | |
| ENST00000227322.7:c.1179+667G>A | ENSP00000227322.3:n.1179+667G>A | |
| ENST00000429220.5:c.958+667G>A | ||
| ENST00000444935.5:c.1091+1428G>A | ||
| NM_003904.3:c.1179+667G>A | NP_003895.1:n.1179+667G>A | |
| NM_001317086.1:c.1017+667G>A | NP_001304015.1:n.1017+667G>A | |
| NM_003904.4:c.1179+667G>A | NP_003895.1:n.1179+667G>A | |
| XR_001748023.2:n.2507+667G>A | ||
| NM_003904.5:c.1179+667G>A MANE Select | NP_003895.1:n.1179+667G>A | |
| NM_001317086.2:c.1017+667G>A | NP_001304015.1:n.1017+667G>A |