Linked Data
MyVariant Identifiers:
chrX:g.154250687T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022412T>C , CM000685.2:g.155022412T>C | GRCh38 |
| NC_000023.10:g.154250687T>C , CM000685.1:g.154250687T>C | GRCh37 |
| NC_000023.9:g.153903881T>C | NCBI36 |
| NG_011403.1:g.5312A>G | |
| NG_011403.2:g.5312A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.141A>G MANE Select | ENSP00000353393.4:p.Ala47= | |
| ENST00000647125.1:c.121+20A>G | ENSP00000496062.1:n.121+20A>G | |
| ENST00000360256.8:c.141A>G | ENSP00000353393.4:p.Ala47= | |
| ENST00000423959.5:c.38+4368A>G | ENSP00000409446.1:n.38+4368A>G | |
| ENST00000453950.1:c.123A>G | ENSP00000389153.1:p.Ala41= | |
| NM_000132.3:c.141A>G | NP_000123.1:p.Ala47= | |
| XM_011531126.1:c.38+4368A>G | XP_011529428.1:n.38+4368A>G | |
| NM_000132.4:c.141A>G MANE Select | NP_000123.1:p.Ala47= |