Linked Data
gnomAD v4:
10-133527171-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133527171C>T , CM000672.2:g.133527171C>T | GRCh38 |
| NC_000010.10:g.135340675C>T , CM000672.1:g.135340675C>T | GRCh37 |
| NC_000010.9:g.135190665C>T | NCBI36 |
| NG_008383.1:g.4809C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463117.6:c.-39-186C>T | ENSP00000440689.1:n.-39-186C>T | |
| ENST00000541261.1:c.-39-186C>T | ENSP00000437799.1:n.-39-186C>T |