Linked Data
gnomAD v4:
4-73404231-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404231T>C , CM000666.2:g.73404231T>C | GRCh38 |
| NC_000004.11:g.74269948T>C , CM000666.1:g.74269948T>C | GRCh37 |
| NC_000004.10:g.74488812T>C | NCBI36 |
| NG_009291.1:g.4977T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000441319.5:c.48-138T>C | ENSP00000392541.1:n.48-138T>C |