Linked Data
MyVariant Identifiers:
chrX:g.154130381A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154902106A>T , CM000685.2:g.154902106A>T | GRCh38 |
| NC_000023.10:g.154130381A>T , CM000685.1:g.154130381A>T | GRCh37 |
| NC_000023.9:g.153783575A>T | NCBI36 |
| NG_011403.1:g.125618T>A | |
| NG_011403.2:g.125618T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6060T>A MANE Select | ENSP00000353393.4:p.Leu2020= | |
| ENST00000360256.8:c.6060T>A | ENSP00000353393.4:p.Leu2020= | |
| NM_000132.3:c.6060T>A | NP_000123.1:p.Leu2020= | |
| XM_011531126.1:c.5955T>A | XP_011529428.1:p.Leu1985= | |
| NM_000132.4:c.6060T>A MANE Select | NP_000123.1:p.Leu2020= |