Linked Data
dbSNP Id:
rs768877252
ExAC:
5:148388597 G / C
gnomAD v2:
5-148388597-G-C
gnomAD v4:
5-149009034-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149009034G>C , CM000667.2:g.149009034G>C | GRCh38 |
| NC_000005.9:g.148388597G>C , CM000667.1:g.148388597G>C | GRCh37 |
| NC_000005.8:g.148368790G>C | NCBI36 |
| NG_007947.2:g.59141C>G , LRG_269:g.59141C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.3224-33C>G | ||
| ENST00000515425.6:c.3328-33C>G MANE Select | ENSP00000423660.1:n.3328-33C>G | |
| ENST00000675793.1:c.*2612-33C>G | ENSP00000502039.1:n.*2612-33C>G | |
| ENST00000323829.9:c.*2716-33C>G | ENSP00000313025.5:n.*2716-33C>G | |
| ENST00000504517.5:c.2858-33C>G | ENSP00000421779.1:n.2858-33C>G | |
| ENST00000504690.5:c.3328-33C>G | ENSP00000425627.1:n.3328-33C>G | |
| ENST00000510779.1:c.2378-33C>G | ||
| ENST00000512049.5:c.3307-33C>G | ENSP00000421860.1:n.3307-33C>G | |
| ENST00000515425.5:c.3328-33C>G | ENSP00000423660.1:n.3328-33C>G | |
| NM_024577.3:c.3328-33C>G , LRG_269t1:c.3328-33C>G | NP_078853.2:n.3328-33C>G | |
| NM_024577.4:c.3328-33C>G MANE Select | NP_078853.2:n.3328-33C>G |