Linked Data
gnomAD v4:
6-39048805-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.39048805A>T , CM000668.2:g.39048805A>T | GRCh38 |
| NC_000006.11:g.39016581A>T , CM000668.1:g.39016581A>T | GRCh37 |
| NC_000006.10:g.39124559A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373256.5:c.-36A>T MANE Select | ENSP00000362353.4:n.-36A>T | |
| ENST00000373256.4:c.-36A>T | ENSP00000362353.4:n.-36A>T | |
| NM_002062.3:c.-36A>T | NP_002053.3:n.-36A>T | |
| XR_926153.1:n.25A>T | ||
| XR_926154.1:n.25A>T | ||
| XR_926155.1:n.25A>T | ||
| NM_002062.4:c.-36A>T | NP_002053.3:n.-36A>T | |
| NR_136562.1:n.25A>T | ||
| NR_136563.1:n.25A>T | ||
| NM_002062.5:c.-36A>T MANE Select | NP_002053.3:n.-36A>T | |
| NR_136562.2:n.25A>T | ||
| NR_136563.2:n.25A>T |