Linked Data
ClinVar Variation Id:
304722
ClinVar RCV Id:
RCV000391699
dbSNP Id:
rs150274138
gnomAD v2:
11-45826700-C-T
gnomAD v3:
11-45805149-C-T
gnomAD v4:
11-45805149-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45805149C>T , CM000673.2:g.45805149C>T | GRCh38 |
| NC_000011.9:g.45826700C>T , CM000673.1:g.45826700C>T | GRCh37 |
| NC_000011.8:g.45783276C>T | NCBI36 |
| NG_009875.1:g.6078C>T , LRG_107:g.6078C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526817.2:c.-31-661C>T | ENSP00000432145.2:n.-31-661C>T | |
| ENST00000314134.4:c.-653C>T MANE Select | ENSP00000313318.3:n.-653C>T | |
| ENST00000314134.3:c.-653C>T | ENSP00000313318.3:n.-653C>T | |
| ENST00000442528.2:c.-32+632C>T | ENSP00000412408.2:n.-32+632C>T | |
| ENST00000526817.1:c.-31-661C>T | ENSP00000432145.1:n.-31-661C>T | |
| ENST00000530471.1:c.-199C>T | ENSP00000432669.1:n.-199C>T | |
| NM_001145265.1:c.-32+632C>T | NP_001138737.1:n.-32+632C>T | |
| NM_001145266.1:c.-31-661C>T | NP_001138738.1:n.-31-661C>T | |
| NM_018389.4:c.-653C>T , LRG_107t1:c.-653C>T | NP_060859.4:n.-653C>T | |
| XM_011520203.1:c.-653C>T | XP_011518505.1:n.-653C>T | |
| XM_011520203.3:c.-653C>T | XP_011518505.1:n.-653C>T | |
| NM_001145265.2:c.-32+632C>T | NP_001138737.1:n.-32+632C>T | |
| NM_018389.5:c.-653C>T MANE Select | NP_060859.4:n.-653C>T |