Linked Data
gnomAD v4:
12-52520387-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520387G>T , CM000674.2:g.52520387G>T | GRCh38 |
| NC_000012.11:g.52914171G>T , CM000674.1:g.52914171G>T | GRCh37 |
| NC_000012.10:g.51200438G>T | NCBI36 |
| NG_008297.1:g.5073C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.-91C>A MANE Select | ENSP00000252242.4:n.-91C>A | |
| ENST00000252242.8:c.-91C>A | ENSP00000252242.4:n.-91C>A | |
| ENST00000546577.1:c.-13+10C>A | ENSP00000449651.1:n.-13+10C>A | |
| ENST00000551275.1:c.-91C>A | ENSP00000448041.1:n.-91C>A | |
| ENST00000552629.5:n.8C>A | ||
| NM_000424.3:c.-91C>A | NP_000415.2:n.-91C>A | |
| NM_000424.4:c.-91C>A MANE Select | NP_000415.2:n.-91C>A |