Linked Data
MyVariant Identifiers:
chrX:g.135741472A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659313A>T , CM000685.2:g.136659313A>T | GRCh38 |
| NC_000023.10:g.135741472A>T , CM000685.1:g.135741472A>T | GRCh37 |
| NC_000023.9:g.135569138A>T | NCBI36 |
| NG_007280.1:g.16137A>T , LRG_141:g.16137A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*302A>T | ENSP00000512122.1:n.*302A>T | |
| ENST00000695725.1:c.*239A>T | ENSP00000512123.1:n.*239A>T | |
| ENST00000695726.1:n.2652A>T | ||
| ENST00000695729.1:n.3487A>T | ||
| ENST00000370629.7:c.684A>T MANE Select | ENSP00000359663.2:p.Val228= | |
| ENST00000370628.2:c.621A>T | ENSP00000359662.2:p.Val207= | |
| ENST00000370629.6:c.684A>T | ENSP00000359663.2:p.Val228= | |
| NM_000074.2:c.684A>T , LRG_141t1:c.684A>T | NP_000065.1:p.Val228= | |
| NM_000074.3:c.684A>T MANE Select | NP_000065.1:p.Val228= |