Linked Data
dbSNP Id:
rs1287830025
gnomAD v2:
19-13346285-A-G
gnomAD v3:
19-13235471-A-G
gnomAD v4:
19-13235471-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13235471A>G , CM000681.2:g.13235471A>G | GRCh38 |
| NC_000019.9:g.13346285A>G , CM000681.1:g.13346285A>G | GRCh37 |
| NC_000019.8:g.13207285A>G | NCBI36 |
| NG_011569.1:g.275990T>C , LRG_7:g.275990T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360228.11:c.5067+143T>C MANE Select | ENSP00000353362.5:n.5067+143T>C | |
| ENST00000573710.7:c.5073+143T>C | ENSP00000460092.3:n.5073+143T>C | |
| ENST00000573891.6:c.486+143T>C | ||
| ENST00000574822.6:n.291+143T>C | ||
| ENST00000585802.6:c.228+143T>C | ENSP00000465598.2:n.228+143T>C | |
| ENST00000593267.2:n.272+143T>C | ||
| ENST00000635727.1:c.5070+143T>C | ENSP00000490001.1:n.5070+143T>C | |
| ENST00000635742.1:n.1056+143T>C | ||
| ENST00000635895.1:c.5070+143T>C | ENSP00000490323.1:n.5070+143T>C | |
| ENST00000636012.1:c.5070+143T>C | ENSP00000490223.1:n.5070+143T>C | |
| ENST00000636058.1:c.382+143T>C | ||
| ENST00000636389.1:c.5070+143T>C | ENSP00000489992.1:n.5070+143T>C | |
| ENST00000636473.1:c.228+143T>C | ENSP00000490173.1:n.228+143T>C | |
| ENST00000636549.1:c.5076+143T>C | ENSP00000490578.1:n.5076+143T>C | |
| ENST00000637276.1:c.5070+143T>C | ENSP00000489777.1:n.5070+143T>C | |
| ENST00000637297.1:c.363+143T>C | ENSP00000489692.1:n.363+143T>C | |
| ENST00000637432.1:c.5085+143T>C | ENSP00000490617.1:n.5085+143T>C | |
| ENST00000637736.1:c.4929+143T>C | ENSP00000489861.1:n.4929+143T>C | |
| ENST00000637769.1:c.5070+143T>C | ENSP00000489778.1:n.5070+143T>C | |
| ENST00000637777.1:c.327+143T>C | ||
| ENST00000637809.1:n.460+143T>C | ||
| ENST00000637819.1:c.471+143T>C | ENSP00000490686.1:n.471+143T>C | |
| ENST00000637832.1:n.61+143T>C | ||
| ENST00000637927.1:c.5073+143T>C | ENSP00000489715.1:n.5073+143T>C | |
| ENST00000638009.2:c.5070+143T>C | ENSP00000489913.1:n.5070+143T>C | |
| ENST00000638029.1:c.5085+143T>C | ENSP00000489829.1:n.5085+143T>C | |
| ENST00000664864.1:c.5271+143T>C | ENSP00000499449.1:n.5271+143T>C | |
| ENST00000360228.9:c.5067+143T>C | ENSP00000353362.5:n.5067+143T>C | |
| ENST00000573710.6:c.5070+143T>C | ENSP00000460092.2:n.5070+143T>C | |
| ENST00000573891.5:c.486+143T>C | ||
| ENST00000574822.5:n.291+143T>C | ||
| ENST00000585802.5:c.1125+143T>C | ENSP00000465598.1:n.1125+143T>C | |
| ENST00000587525.5:c.528+143T>C | ENSP00000467729.1:n.528+143T>C | |
| ENST00000593267.1:n.272+143T>C | ||
| ENST00000614285.4:c.5085+143T>C | ENSP00000479983.1:n.5085+143T>C | |
| NM_000068.3:c.5085+143T>C | NP_000059.3:n.5085+143T>C | |
| NM_001127221.1:c.5070+143T>C , LRG_7t1:c.5070+143T>C | NP_001120693.1:n.5070+143T>C | |
| NM_001127222.1:c.5067+143T>C | NP_001120694.1:n.5067+143T>C | |
| NM_001174080.1:c.5076+143T>C | NP_001167551.1:n.5076+143T>C | |
| NM_023035.2:c.5085+143T>C | NP_075461.2:n.5085+143T>C | |
| NM_000068.4:c.5085+143T>C | NP_000059.3:n.5085+143T>C | |
| NM_001127222.2:c.5067+143T>C MANE Select | NP_001120694.1:n.5067+143T>C | |
| NM_001174080.2:c.5076+143T>C | NP_001167551.1:n.5076+143T>C | |
| NM_023035.3:c.5085+143T>C | NP_075461.2:n.5085+143T>C | |
| NM_001127221.2:c.5070+143T>C | NP_001120693.1:n.5070+143T>C |