Linked Data
gnomAD v4:
7-107710202-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107710202A>T , CM000669.2:g.107710202A>T | GRCh38 |
| NC_000007.13:g.107350647A>T , CM000669.1:g.107350647A>T | GRCh37 |
| NC_000007.12:g.107137883A>T | NCBI36 |
| NG_008489.1:g.54568A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2235+3A>T MANE Select | ENSP00000494017.1:n.2235+3A>T | |
| ENST00000644846.1:c.891+3A>T | ||
| ENST00000265715.7:c.2235+3A>T | ENSP00000265715.3:n.2235+3A>T | |
| ENST00000492030.2:n.421+3A>T | ||
| NM_000441.1:c.2235+3A>T | NP_000432.1:n.2235+3A>T | |
| XM_005250425.1:c.2235+3A>T | XP_005250482.1:n.2235+3A>T | |
| XM_005250425.2:c.2235+3A>T | XP_005250482.1:n.2235+3A>T | |
| XM_017012318.1:c.2157+3A>T | XP_016867807.1:n.2157+3A>T | |
| NM_000441.2:c.2235+3A>T MANE Select | NP_000432.1:n.2235+3A>T |