Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919898C>G , CM000679.2:g.74919898C>G | GRCh38 |
| NC_000017.10:g.72915993C>G , CM000679.1:g.72915993C>G | GRCh37 |
| NC_000017.9:g.70427588C>G | NCBI36 |
| NG_007882.1:g.8359G>C | |
| NG_033062.1:g.624C>G | |
| NG_007882.2:g.8366G>C | |
| NG_033062.2:g.624C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614341.5:c.938G>C MANE Select | ENSP00000480279.1:p.Gly313Ala | |
| ENST00000579243.1:c.*537G>C | ENSP00000462568.1:n.*537G>C | |
| ENST00000614341.4:c.938G>C | ENSP00000480279.1:p.Gly313Ala | |
| NM_001282489.2:c.629G>C | NP_001269418.1:p.Gly210Ala | |
| NM_173477.4:c.938G>C | NP_775748.2:p.Gly313Ala | |
| XM_011524296.1:c.629G>C | XP_011522598.1:p.Gly210Ala | |
| XM_011524296.2:c.629G>C | XP_011522598.1:p.Gly210Ala | |
| NM_173477.5:c.938G>C MANE Select | NP_775748.2:p.Gly313Ala | |
| NM_001282489.3:c.629G>C | NP_001269418.1:p.Gly210Ala |