Linked Data
dbSNP Id:
rs1350756707
gnomAD v2:
12-88953880-G-T
gnomAD v3:
12-88560103-G-T
gnomAD v4:
12-88560103-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88560103G>T , CM000674.2:g.88560103G>T | GRCh38 |
| NC_000012.11:g.88953880G>T , CM000674.1:g.88953880G>T | GRCh37 |
| NC_000012.10:g.87478011G>T | NCBI36 |
| NG_012098.1:g.25359C>A | |
| NG_012098.2:g.25359C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000347404.10:c.16-14238C>A | ENSP00000054216.5:n.16-14238C>A | |
| ENST00000644744.1:c.16-14238C>A MANE Select | ENSP00000495951.1:n.16-14238C>A | |
| ENST00000646633.1:c.*17-14238C>A | ENSP00000494139.1:n.*17-14238C>A | |
| ENST00000228280.9:c.16-14238C>A | ENSP00000228280.5:n.16-14238C>A | |
| ENST00000347404.9:c.16-14238C>A | ENSP00000054216.5:n.16-14238C>A | |
| ENST00000357116.4:c.-48+20161C>A | ENSP00000474021.1:n.-48+20161C>A | |
| ENST00000552044.1:c.-139+4105C>A | ENSP00000475042.1:n.-139+4105C>A | |
| NM_000899.4:c.16-14238C>A | NP_000890.1:n.16-14238C>A | |
| NM_003994.5:c.16-14238C>A | NP_003985.2:n.16-14238C>A | |
| NM_000899.5:c.16-14238C>A MANE Select | NP_000890.1:n.16-14238C>A | |
| NM_003994.6:c.16-14238C>A | NP_003985.2:n.16-14238C>A |