Linked Data
gnomAD v4:
4-73404222-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404222T>A , CM000666.2:g.73404222T>A | GRCh38 |
| NC_000004.11:g.74269939T>A , CM000666.1:g.74269939T>A | GRCh37 |
| NC_000004.10:g.74488803T>A | NCBI36 |
| NG_009291.1:g.4968T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000441319.5:c.48-147T>A | ENSP00000392541.1:n.48-147T>A |