Linked Data
MyVariant Identifiers:
chrX:g.135741418T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659259T>C , CM000685.2:g.136659259T>C | GRCh38 |
| NC_000023.10:g.135741418T>C , CM000685.1:g.135741418T>C | GRCh37 |
| NC_000023.9:g.135569084T>C | NCBI36 |
| NG_007280.1:g.16083T>C , LRG_141:g.16083T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*248T>C | ENSP00000512122.1:n.*248T>C | |
| ENST00000695725.1:c.*185T>C | ENSP00000512123.1:n.*185T>C | |
| ENST00000695726.1:n.2598T>C | ||
| ENST00000695729.1:n.3433T>C | ||
| ENST00000370629.7:c.630T>C MANE Select | ENSP00000359663.2:p.Asn210= | |
| ENST00000370628.2:c.567T>C | ENSP00000359662.2:p.Asn189= | |
| ENST00000370629.6:c.630T>C | ENSP00000359663.2:p.Asn210= | |
| NM_000074.2:c.630T>C , LRG_141t1:c.630T>C | NP_000065.1:p.Asn210= | |
| NM_000074.3:c.630T>C MANE Select | NP_000065.1:p.Asn210= |