Linked Data
gnomAD v4:
3-81705507-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705507C>G , CM000665.2:g.81705507C>G | GRCh38 |
| NC_000003.11:g.81754658C>G , CM000665.1:g.81754658C>G | GRCh37 |
| NC_000003.10:g.81837348C>G | NCBI36 |
| NG_011810.1:g.61294G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.250G>C MANE Select | ENSP00000410833.2:p.Gly84Arg | |
| ENST00000429644.6:c.250G>C | ENSP00000410833.2:p.Gly84Arg | |
| ENST00000489715.1:c.127G>C | ENSP00000419638.1:p.Gly43Arg | |
| NM_000158.3:c.250G>C | NP_000149.3:p.Gly84Arg | |
| NM_000158.4:c.250G>C MANE Select | NP_000149.4:p.Gly84Arg |