Linked Data
gnomAD v4:
5-150155871-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150155871A>C , CM000667.2:g.150155871A>C | GRCh38 |
| NC_000005.9:g.149535434A>C , CM000667.1:g.149535434A>C | GRCh37 |
| NC_000005.8:g.149515627A>C | NCBI36 |
| NG_023367.1:g.4989T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000523456.1:n.2T>G | ||
| XM_005268464.2:c.-627T>G | XP_005268521.1:n.-627T>G | |
| XM_011537659.1:c.-948T>G | XP_011535961.1:n.-948T>G |