Linked Data
gnomAD v4:
9-136687409-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136687409C>T , CM000671.2:g.136687409C>T | GRCh38 |
| NC_000009.11:g.139581861C>T , CM000671.1:g.139581861C>T | GRCh37 |
| NC_000009.10:g.138701682C>T | NCBI36 |
| NG_008090.1:g.5051G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.-52G>A MANE Select | ENSP00000360761.2:n.-52G>A | |
| ENST00000371696.6:c.-52G>A | ENSP00000360761.2:n.-52G>A | |
| NM_001012727.1:c.-52G>A | NP_001012745.1:n.-52G>A | |
| NM_006412.3:c.-52G>A | NP_006403.2:n.-52G>A | |
| NM_006412.4:c.-52G>A MANE Select | NP_006403.2:n.-52G>A | |
| NM_001012727.2:c.-52G>A | NP_001012745.1:n.-52G>A |