Linked Data
MyVariant Identifiers:
chrX:g.50658884G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50915884G>C , CM000685.2:g.50915884G>C | GRCh38 |
| NC_000023.10:g.50658884G>C , CM000685.1:g.50658884G>C | GRCh37 |
| NC_000023.9:g.50675624G>C | NCBI36 |
| NG_012894.1:g.10101G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.456G>C MANE Select | ENSP00000252677.3:p.Val152= | |
| ENST00000252677.3:c.456G>C | ENSP00000252677.3:p.Val152= | |
| NM_005448.2:c.456G>C MANE Select | NP_005439.2:p.Val152= |