Linked Data
MyVariant Identifiers:
chrX:g.153035630T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153770175T>C , CM000685.2:g.153770175T>C | GRCh38 |
| NC_000023.10:g.153035630T>C , CM000685.1:g.153035630T>C | GRCh37 |
| NC_000023.9:g.152688824T>C | NCBI36 |
| NG_013255.1:g.10980T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361971.10:c.1713T>C MANE Select | ENSP00000355378.5:p.Ala571= | |
| ENST00000361971.9:c.1713T>C | ENSP00000355378.5:p.Ala571= | |
| ENST00000538966.5:c.1782T>C | ENSP00000442736.1:p.Ala594= | |
| NM_001163257.1:c.1782T>C | NP_001156729.1:p.Ala594= | |
| NM_005393.2:c.1713T>C | NP_005384.2:p.Ala571= | |
| NM_005393.3:c.1713T>C MANE Select | NP_005384.2:p.Ala571= | |
| NM_001163257.2:c.1782T>C | NP_001156729.1:p.Ala594= |