Linked Data
gnomAD v4:
X-48523743-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48523743T>C , CM000685.2:g.48523743T>C | GRCh38 |
| NC_000023.10:g.48382131T>C , CM000685.1:g.48382131T>C | GRCh37 |
| NC_000023.9:g.48267075T>C | NCBI36 |
| NG_007452.1:g.6968T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.-29T>C MANE Select | ENSP00000417052.1:n.-29T>C | |
| ENST00000651615.1:c.-29T>C | ENSP00000498524.1:n.-29T>C | |
| ENST00000276096.10:n.110-180T>C | ||
| ENST00000414061.1:c.-29T>C | ENSP00000405832.1:n.-29T>C | |
| ENST00000446158.5:c.-29T>C | ENSP00000390031.1:n.-29T>C | |
| ENST00000495186.5:c.-29T>C | ENSP00000417052.1:n.-29T>C | |
| ENST00000498425.1:n.104-11T>C | ||
| NM_006579.2:c.-29T>C | NP_006570.1:n.-29T>C | |
| NM_006579.3:c.-29T>C MANE Select | NP_006570.1:n.-29T>C |