Linked Data
MyVariant Identifiers:
chrX:g.37663159G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37803906G>A , CM000685.2:g.37803906G>A | GRCh38 |
| NC_000023.10:g.37663159G>A , CM000685.1:g.37663159G>A | GRCh37 |
| NC_000023.9:g.37548103G>A | NCBI36 |
| NG_009065.1:g.28890G>A , LRG_53:g.28890G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.*436G>A | ENSP00000512461.1:n.*436G>A | |
| ENST00000696171.1:c.831G>A | ENSP00000512462.1:p.Glu277= | |
| ENST00000378588.5:c.927G>A MANE Select | ENSP00000367851.4:p.Glu309= | |
| ENST00000378588.4:c.927G>A | ENSP00000367851.4:p.Glu309= | |
| ENST00000465127.1:c.171+377906G>A | ENSP00000417050.1:n.171+377906G>A | |
| ENST00000492288.1:n.352G>A | ||
| NM_000397.3:c.927G>A , LRG_53t1:c.927G>A | NP_000388.2:p.Glu309= | |
| XM_011543890.1:c.621G>A | XP_011542192.1:p.Glu207= | |
| NM_000397.4:c.927G>A MANE Select | NP_000388.2:p.Glu309= |