Linked Data
ClinVar Variation Id:
2929268
ClinVar RCV Id:
RCV003781994
MyVariant Identifiers:
chrX:g.30322810A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30304693A>G , CM000685.2:g.30304693A>G | GRCh38 |
| NC_000023.10:g.30322810A>G , CM000685.1:g.30322810A>G | GRCh37 |
| NC_000023.9:g.30232731A>G | NCBI36 |
| NG_009814.1:g.9686T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1299T>C MANE Select | ENSP00000368253.4:p.Leu433= | |
| ENST00000378970.4:c.1299T>C | ENSP00000368253.4:p.Leu433= | |
| NM_000475.4:c.1299T>C | NP_000466.2:p.Leu433= | |
| NM_000475.5:c.1299T>C MANE Select | NP_000466.2:p.Leu433= |