Linked Data
gnomAD v4:
1-93998099-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93998099C>G , CM000663.2:g.93998099C>G | GRCh38 |
| NC_000001.10:g.94463655C>G , CM000663.1:g.94463655C>G | GRCh37 |
| NC_000001.9:g.94236243C>G | NCBI36 |
| NG_009073.1:g.128051G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6491G>C MANE Select | ENSP00000359245.3:p.Gly2164Ala | |
| ENST00000370225.3:c.6491G>C | ENSP00000359245.3:p.Gly2164Ala | |
| ENST00000536513.5:c.2867G>C | ENSP00000439707.2:p.Gly956Ala | |
| NM_000350.2:c.6491G>C | NP_000341.2:p.Gly2164Ala | |
| NM_000350.3:c.6491G>C MANE Select | NP_000341.2:p.Gly2164Ala |