Linked Data
MyVariant Identifiers:
chrX:g.48385396A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527008A>C , CM000685.2:g.48527008A>C | GRCh38 |
| NC_000023.10:g.48385396A>C , CM000685.1:g.48385396A>C | GRCh37 |
| NC_000023.9:g.48270340A>C | NCBI36 |
| NG_007452.1:g.10233A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.321A>C MANE Select | ENSP00000417052.1:p.Gly107= | |
| ENST00000651615.1:c.321A>C | ENSP00000498524.1:p.Gly107= | |
| ENST00000276096.10:n.279A>C | ||
| ENST00000414061.1:c.321A>C | ENSP00000405832.1:p.Gly107= | |
| ENST00000446158.5:c.321A>C | ENSP00000390031.1:p.Gly107= | |
| ENST00000466461.1:n.160A>C | ||
| ENST00000495186.5:c.321A>C | ENSP00000417052.1:p.Gly107= | |
| ENST00000498425.1:n.442A>C | ||
| NM_006579.2:c.321A>C | NP_006570.1:p.Gly107= | |
| NM_006579.3:c.321A>C MANE Select | NP_006570.1:p.Gly107= |