Linked Data
gnomAD v4:
X-50192579-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50192579C>A , CM000685.2:g.50192579C>A | GRCh38 |
| NC_000023.10:g.49957230C>A , CM000685.1:g.49957230C>A | GRCh37 |
| NC_000023.9:g.49843970C>A | NCBI36 |
| NG_012552.1:g.13435G>T | |
| NG_012552.2:g.13435G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.2134G>T MANE Select | ENSP00000351327.2:p.Ala712Ser | |
| ENST00000358526.6:c.2134G>T | ENSP00000351327.2:p.Ala712Ser | |
| ENST00000376064.7:c.2107G>T | ENSP00000365232.3:p.Ala703Ser | |
| ENST00000481402.5:n.2246G>T | ||
| NM_003886.2:c.2134G>T | NP_003877.2:p.Ala712Ser | |
| NM_139289.1:c.2107G>T | NP_647450.1:p.Ala703Ser | |
| NM_003886.3:c.2134G>T MANE Select | NP_003877.2:p.Ala712Ser | |
| NM_139289.2:c.2107G>T | NP_647450.1:p.Ala703Ser |