Linked Data
MyVariant Identifiers:
chrX:g.77369364A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78113867A>T , CM000685.2:g.78113867A>T | GRCh38 |
| NC_000023.10:g.77369364A>T , CM000685.1:g.77369364A>T | GRCh37 |
| NC_000023.9:g.77256020A>T | NCBI36 |
| NG_008862.1:g.14699A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.240A>T MANE Select | ENSP00000362413.4:p.Pro80= | |
| ENST00000644362.1:c.156A>T | ENSP00000496140.1:p.Pro52= | |
| ENST00000373316.4:c.240A>T | ENSP00000362413.4:p.Pro80= | |
| ENST00000491291.1:n.232A>T | ||
| NM_000291.3:c.240A>T | NP_000282.1:p.Pro80= | |
| NM_000291.4:c.240A>T MANE Select | NP_000282.1:p.Pro80= |