Linked Data
ClinVar Variation Id:
424934
dbSNP Id:
rs1064797134
gnomAD v3:
1-215878800-C-T
gnomAD v4:
1-215878800-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215878800C>T , CM000663.2:g.215878800C>T | GRCh38 |
| NC_000001.10:g.216052142C>T , CM000663.1:g.216052142C>T | GRCh37 |
| NC_000001.9:g.214118765C>T | NCBI36 |
| NG_009497.1:g.549597G>A | |
| NG_009497.2:g.549649G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.8522G>A MANE Select | ENSP00000305941.3:p.Trp2841Ter | |
| ENST00000674083.1:c.8522G>A | ENSP00000501296.1:p.Trp2841Ter | |
| ENST00000307340.7:c.8522G>A | ENSP00000305941.3:p.Trp2841Ter | |
| NM_206933.2:c.8522G>A | NP_996816.2:p.Trp2841Ter | |
| NM_206933.3:c.8522G>A | NP_996816.2:p.Trp2841Ter | |
| NM_206933.4:c.8522G>A MANE Select | NP_996816.3:p.Trp2841Ter |