Linked Data
MyVariant Identifiers:
chrX:g.153035612G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153770157G>T , CM000685.2:g.153770157G>T | GRCh38 |
| NC_000023.10:g.153035612G>T , CM000685.1:g.153035612G>T | GRCh37 |
| NC_000023.9:g.152688806G>T | NCBI36 |
| NG_013255.1:g.10962G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361971.10:c.1695G>T MANE Select | ENSP00000355378.5:p.Gly565= | |
| ENST00000361971.9:c.1695G>T | ENSP00000355378.5:p.Gly565= | |
| ENST00000538966.5:c.1764G>T | ENSP00000442736.1:p.Gly588= | |
| NM_001163257.1:c.1764G>T | NP_001156729.1:p.Gly588= | |
| NM_005393.2:c.1695G>T | NP_005384.2:p.Gly565= | |
| NM_005393.3:c.1695G>T MANE Select | NP_005384.2:p.Gly565= | |
| NM_001163257.2:c.1764G>T | NP_001156729.1:p.Gly588= |