Linked Data
ClinVar Variation Id:
527102
dbSNP Id:
rs1212611138
gnomAD v2:
11-2593238-C-T
gnomAD v3:
11-2572008-C-T
gnomAD v4:
11-2572008-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2572008C>T , CM000673.2:g.2572008C>T | GRCh38 |
| NC_000011.9:g.2593238C>T , CM000673.1:g.2593238C>T | GRCh37 |
| NC_000011.8:g.2549814C>T | NCBI36 |
| NG_008935.1:g.132018C>T , LRG_287:g.132018C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.423-5C>T | ENSP00000434560.2:n.423-5C>T | |
| ENST00000646564.2:c.478-11427C>T | ENSP00000495806.2:n.478-11427C>T | |
| ENST00000155840.12:c.684-5C>T MANE Select | ENSP00000155840.2:n.684-5C>T | |
| ENST00000335475.6:c.303-5C>T | ENSP00000334497.5:n.303-5C>T | |
| ENST00000646564.1:c.124-11427C>T | ENSP00000495806.1:n.124-11427C>T | |
| ENST00000155840.9:c.684-5C>T | ENSP00000155840.2:n.684-5C>T | |
| ENST00000335475.5:c.303-5C>T | ENSP00000334497.5:n.303-5C>T | |
| ENST00000496887.6:c.423-5C>T | ENSP00000434560.1:n.423-5C>T | |
| NM_000218.2:c.684-5C>T , LRG_287t1:c.684-5C>T | NP_000209.2:n.684-5C>T | |
| NM_181798.1:c.303-5C>T , LRG_287t2:c.303-5C>T | NP_861463.1:n.303-5C>T | |
| NM_000218.3:c.684-5C>T MANE Select | NP_000209.2:n.684-5C>T |