Linked Data
gnomAD v4:
7-95324611-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95324611T>C , CM000669.2:g.95324611T>C | GRCh38 |
| NC_000007.13:g.94953923T>C , CM000669.1:g.94953923T>C | GRCh37 |
| NC_000007.12:g.94791859T>C | NCBI36 |
| NG_008779.1:g.4962A>G | |
| NG_008779.2:g.5096A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222381.7:c.-136A>G | ENSP00000222381.3:n.-136A>G | |
| NM_000446.6:c.-136A>G | NP_000437.3:n.-136A>G |