Linked Data
MyVariant Identifiers:
chrX:g.154194260A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154965985A>C , CM000685.2:g.154965985A>C | GRCh38 |
| NC_000023.10:g.154194260A>C , CM000685.1:g.154194260A>C | GRCh37 |
| NC_000023.9:g.153847454A>C | NCBI36 |
| NG_011403.1:g.61739T>G | |
| NG_011403.2:g.61739T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1428T>G MANE Select | ENSP00000353393.4:p.Val476= | |
| ENST00000647125.1:c.*1304T>G | ENSP00000496062.1:n.*1304T>G | |
| ENST00000360256.8:c.1428T>G | ENSP00000353393.4:p.Val476= | |
| ENST00000483822.2:n.248T>G | ||
| NM_000132.3:c.1428T>G | NP_000123.1:p.Val476= | |
| XM_011531126.1:c.1323T>G | XP_011529428.1:p.Val441= | |
| NM_000132.4:c.1428T>G MANE Select | NP_000123.1:p.Val476= |