Linked Data
gnomAD v4:
4-73404258-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404258A>T , CM000666.2:g.73404258A>T | GRCh38 |
| NC_000004.11:g.74269975A>T , CM000666.1:g.74269975A>T | GRCh37 |
| NC_000004.10:g.74488839A>T | NCBI36 |
| NG_009291.1:g.5004A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295897.8:c.-70A>T | ENSP00000295897.4:n.-70A>T | |
| ENST00000441319.5:c.48-111A>T | ENSP00000392541.1:n.48-111A>T | |
| ENST00000621628.4:c.-70A>T | ENSP00000480485.1:n.-70A>T | |
| NM_000477.5:c.-70A>T | NP_000468.1:n.-70A>T | |
| NM_000477.6:c.-70A>T | NP_000468.1:n.-70A>T |