Linked Data
gnomAD v4:
5-10286452-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.10286452G>C , CM000667.2:g.10286452G>C | GRCh38 |
| NC_000005.9:g.10286564G>C , CM000667.1:g.10286564G>C | GRCh37 |
| NC_000005.8:g.10339564G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296658.4:c.368C>G MANE Select | ENSP00000296658.3:p.Ala123Gly | |
| ENST00000296658.3:c.368C>G | ENSP00000296658.3:p.Ala123Gly | |
| ENST00000506821.1:n.622C>G | ||
| ENST00000510532.5:n.436C>G | ||
| ENST00000511963.5:n.476C>G | ||
| NM_138809.3:c.368C>G | NP_620164.1:p.Ala123Gly | |
| NM_138809.4:c.368C>G MANE Select | NP_620164.1:p.Ala123Gly |