Linked Data
MyVariant Identifiers:
chrX:g.37587097T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37727844T>C , CM000685.2:g.37727844T>C | GRCh38 |
| NC_000023.10:g.37587097T>C , CM000685.1:g.37587097T>C | GRCh37 |
| NC_000023.9:g.37472036T>C | NCBI36 |
| NG_007473.1:g.46985T>C | |
| NG_007473.3:g.46965T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378616.5:c.717T>C MANE Select | ENSP00000367879.3:p.Val239= | |
| ENST00000378616.3:c.717T>C | ENSP00000367879.3:p.Val239= | |
| ENST00000465127.1:c.171+301844T>C | ENSP00000417050.1:n.171+301844T>C | |
| NM_021083.2:c.717T>C | NP_066569.1:p.Val239= | |
| NM_021083.4:c.717T>C MANE Select | NP_066569.1:p.Val239= |