Linked Data
MyVariant Identifiers:
chrX:g.154250798A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022523A>G , CM000685.2:g.155022523A>G | GRCh38 |
| NC_000023.10:g.154250798A>G , CM000685.1:g.154250798A>G | GRCh37 |
| NC_000023.9:g.153903992A>G | NCBI36 |
| NG_011403.1:g.5201T>C | |
| NG_011403.2:g.5201T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.30T>C MANE Select | ENSP00000353393.4:p.Phe10= | |
| ENST00000647125.1:c.30T>C | ENSP00000496062.1:p.Phe10= | |
| ENST00000360256.8:c.30T>C | ENSP00000353393.4:p.Phe10= | |
| ENST00000423959.5:c.38+4257T>C | ENSP00000409446.1:n.38+4257T>C | |
| ENST00000453950.1:c.39-27T>C | ENSP00000389153.1:n.39-27T>C | |
| NM_000132.3:c.30T>C | NP_000123.1:p.Phe10= | |
| XM_011531126.1:c.38+4257T>C | XP_011529428.1:n.38+4257T>C | |
| NM_000132.4:c.30T>C MANE Select | NP_000123.1:p.Phe10= |