Linked Data
gnomAD v4:
7-155812383-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155812383A>C , CM000669.2:g.155812383A>C | GRCh38 |
| NC_000007.13:g.155605077A>C , CM000669.1:g.155605077A>C | GRCh37 |
| NC_000007.12:g.155297838A>C | NCBI36 |
| NG_007504.2:g.4891T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297261.7:c.-261T>G MANE Select | ENSP00000297261.2:n.-261T>G | |
| NM_000193.4:c.-261T>G MANE Select | NP_000184.1:n.-261T>G |