Linked Data
gnomAD v4:
12-51912328-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51912328C>T , CM000674.2:g.51912328C>T | GRCh38 |
| NC_000012.11:g.52306112C>T , CM000674.1:g.52306112C>T | GRCh37 |
| NC_000012.10:g.50592379C>T | NCBI36 |
| NG_009549.1:g.9911C>T , LRG_543:g.9911C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551576.6:c.-5-142C>T | ENSP00000455848.2:n.-5-142C>T | |
| ENST00000552678.2:c.-5-142C>T | ENSP00000457394.2:n.-5-142C>T | |
| ENST00000388922.9:c.-5-142C>T MANE Select | ENSP00000373574.4:n.-5-142C>T | |
| ENST00000388922.8:c.-5-142C>T | ENSP00000373574.4:n.-5-142C>T | |
| ENST00000551576.5:c.-5-142C>T | ENSP00000455848.1:n.-5-142C>T | |
| NM_000020.2:c.-5-142C>T , LRG_543t1:c.-5-142C>T | NP_000011.2:n.-5-142C>T | |
| XM_005269235.2:c.-5-142C>T | XP_005269292.1:n.-5-142C>T | |
| NM_000020.3:c.-5-142C>T MANE Select | NP_000011.2:n.-5-142C>T |