Linked Data
gnomAD v4:
5-132369660-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132369660T>C , CM000667.2:g.132369660T>C | GRCh38 |
| NC_000005.9:g.131705352T>C , CM000667.1:g.131705352T>C | GRCh37 |
| NC_000005.8:g.131733251T>C | NCBI36 |
| NG_008982.1:g.4952T>C | |
| NG_008982.2:g.4957T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110997.1:n.73+184A>G |