Linked Data
gnomAD v4:
9-21140607-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21140607C>A , CM000671.2:g.21140607C>A | GRCh38 |
| NC_000009.11:g.21140606C>A , CM000671.1:g.21140606C>A | GRCh37 |
| NC_000009.10:g.21130606C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380229.3:c.*376G>T | ENSP00000369578.2:n.*376G>T |