gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.24261089 (NFE)
Genomes Max Group AF
0.24289612 (NFE)
Exomes Max Group AF
0.201346 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112153104C>G , CM000673.2:g.112153104C>G | GRCh38 |
| NC_000011.9:g.112023827C>G , CM000673.1:g.112023827C>G | GRCh37 |
| NC_000011.8:g.111529037C>G | NCBI36 |
| NG_028143.1:g.16014G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000280357.12:c.91+488G>C MANE Select | ENSP00000280357.7:n.91+488G>C | |
| ENST00000280357.11:c.91+488G>C | ENSP00000280357.7:n.91+488G>C | |
| ENST00000524595.5:c.79+1871G>C | ENSP00000434561.1:n.79+1871G>C | |
| ENST00000525987.5:n.320-17315C>G | ||
| ENST00000528832.1:c.91+488G>C | ENSP00000434161.1:n.91+488G>C | |
| ENST00000531744.5:c.315-17315C>G | ENSP00000456957.1:n.315-17315C>G | |
| ENST00000532699.1:c.315-17315C>G | ENSP00000456434.1:n.315-17315C>G | |
| ENST00000533858.5:n.278+1871G>C | ||
| ENST00000534225.1:n.775G>C | ||
| NM_001243211.1:c.79+1871G>C | NP_001230140.1:n.79+1871G>C | |
| NM_001562.3:c.91+488G>C | NP_001553.1:n.91+488G>C | |
| XM_011542805.1:c.79+1871G>C | XP_011541107.1:n.79+1871G>C | |
| XM_011542806.1:c.91+488G>C | XP_011541108.1:n.91+488G>C | |
| XM_011542806.2:c.91+488G>C | XP_011541108.1:n.91+488G>C | |
| NM_001562.4:c.91+488G>C MANE Select | NP_001553.1:n.91+488G>C | |
| NM_001243211.2:c.79+1871G>C | NP_001230140.1:n.79+1871G>C | |
| NM_001386420.1:c.91+488G>C | NP_001373349.1:n.91+488G>C |