Linked Data
gnomAD v4:
7-155812328-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155812328C>T , CM000669.2:g.155812328C>T | GRCh38 |
| NC_000007.13:g.155605022C>T , CM000669.1:g.155605022C>T | GRCh37 |
| NC_000007.12:g.155297783C>T | NCBI36 |
| NG_007504.2:g.4946G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297261.7:c.-206G>A MANE Select | ENSP00000297261.2:n.-206G>A | |
| NM_000193.4:c.-206G>A MANE Select | NP_000184.1:n.-206G>A |