Linked Data
MyVariant Identifiers:
chrX:g.25031380C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013263C>A , CM000685.2:g.25013263C>A | GRCh38 |
| NC_000023.10:g.25031380C>A , CM000685.1:g.25031380C>A | GRCh37 |
| NC_000023.9:g.24941301C>A | NCBI36 |
| NG_008281.1:g.7686G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.732G>T MANE Select | ENSP00000368332.4:p.Leu244= | |
| ENST00000379044.4:c.732G>T | ENSP00000368332.4:p.Leu244= | |
| NM_139058.2:c.732G>T | NP_620689.1:p.Leu244= | |
| NM_139058.3:c.732G>T MANE Select | NP_620689.1:p.Leu244= |