Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30993206T>G , CM000678.2:g.30993206T>G | GRCh38 |
| NC_000016.9:g.31004527T>G , CM000678.1:g.31004527T>G | GRCh37 |
| NC_000016.8:g.30912028T>G | NCBI36 |
| NG_041829.1:g.22303A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215095.11:c.710A>C MANE Select | ENSP00000215095.5:p.Glu237Ala | |
| ENST00000565419.2:c.710A>C | ENSP00000455899.1:p.Glu237Ala | |
| ENST00000215095.9:c.710A>C | ENSP00000215095.5:p.Glu237Ala | |
| ENST00000565419.1:c.710A>C | ENSP00000455899.1:p.Glu237Ala | |
| ENST00000569638.5:c.458A>C | ENSP00000457067.1:p.Glu153Ala | |
| NM_052874.4:c.710A>C | NP_443106.1:p.Glu237Ala | |
| XM_017022893.1:c.692A>C | XP_016878382.1:p.Glu231Ala | |
| NM_052874.5:c.710A>C MANE Select | NP_443106.1:p.Glu237Ala |