Linked Data
dbSNP Id:
rs1245322725
gnomAD v2:
3-8787563-G-A
gnomAD v3:
3-8745877-G-A
gnomAD v4:
3-8745877-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745877G>A , CM000665.2:g.8745877G>A | GRCh38 |
| NC_000003.11:g.8787563G>A , CM000665.1:g.8787563G>A | GRCh37 |
| NC_000003.10:g.8762563G>A | NCBI36 |
| NG_008797.2:g.17068G>A , LRG_329:g.17068G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343849.3:c.*10G>A MANE Select | ENSP00000341940.2:n.*10G>A | |
| ENST00000343849.2:c.*10G>A | ENSP00000341940.2:n.*10G>A | |
| ENST00000397368.2:c.*6+4G>A | ENSP00000380525.2:n.*6+4G>A | |
| ENST00000472766.1:n.155+11887G>A | ||
| NM_001234.4:c.*6+4G>A | NP_001225.1:n.*6+4G>A | |
| NM_033337.2:c.*10G>A , LRG_329t1:c.*10G>A | NP_203123.1:n.*10G>A | |
| NM_001234.5:c.*6+4G>A | NP_001225.1:n.*6+4G>A | |
| NM_033337.3:c.*10G>A MANE Select | NP_203123.1:n.*10G>A |