Linked Data
MyVariant Identifiers:
chrX:g.30326685G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30308568G>A , CM000685.2:g.30308568G>A | GRCh38 |
| NC_000023.10:g.30326685G>A , CM000685.1:g.30326685G>A | GRCh37 |
| NC_000023.9:g.30236606G>A | NCBI36 |
| NG_009814.1:g.5811C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.796C>T MANE Select | ENSP00000368253.4:p.Leu266= | |
| ENST00000378970.4:c.796C>T | ENSP00000368253.4:p.Leu266= | |
| NM_000475.4:c.796C>T | NP_000466.2:p.Leu266= | |
| NM_000475.5:c.796C>T MANE Select | NP_000466.2:p.Leu266= |