Linked Data
gnomAD v4:
X-21845346-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21845346T>C , CM000685.2:g.21845346T>C | GRCh38 |
| NC_000023.10:g.21863464T>C , CM000685.1:g.21863464T>C | GRCh37 |
| NC_000023.9:g.21773385T>C | NCBI36 |
| NG_012797.1:g.10809T>C | |
| NG_012797.2:g.10809T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379484.10:c.400T>C MANE Select | ENSP00000368798.5:p.Ser134Pro | |
| ENST00000365779.2:c.400T>C | ENSP00000368796.1:p.Ser134Pro | |
| ENST00000379484.9:c.400T>C | ENSP00000368798.5:p.Ser134Pro | |
| ENST00000465888.1:n.499T>C | ||
| NM_015884.3:c.400T>C | NP_056968.1:p.Ser134Pro | |
| NM_015884.4:c.400T>C MANE Select | NP_056968.1:p.Ser134Pro |