Linked Data
gnomAD v4:
6-29941947-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29941947T>C , CM000668.2:g.29941947T>C | GRCh38 |
| NC_000006.11:g.29909724T>C , CM000668.1:g.29909724T>C | GRCh37 |
| NC_000006.10:g.30017703T>C | NCBI36 |
| NG_029217.2:g.4485T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396634.5:c.-281-19T>C | ENSP00000379873.1:n.-281-19T>C |