Linked Data
gnomAD v4:
4-99352901-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99352901T>C , CM000666.2:g.99352901T>C | GRCh38 |
| NC_000004.11:g.100274058T>C , CM000666.1:g.100274058T>C | GRCh37 |
| NC_000004.10:g.100493081T>C | NCBI36 |
| NG_011718.1:g.4860A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515683.5:c.-226A>G | ENSP00000426083.1:n.-226A>G | |
| NM_000669.4:c.-226A>G | NP_000660.1:n.-226A>G | |
| NR_133005.1:n.145A>G | ||
| XM_011531588.1:c.-226A>G | XP_011529890.1:n.-226A>G | |
| XM_011531589.1:c.-466A>G | XP_011529891.1:n.-466A>G |