Linked Data
ClinVar Variation Id:
2661864
ClinVar RCV Id:
RCV003436893
MyVariant Identifiers:
chrX:g.154132328A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904053A>G , CM000685.2:g.154904053A>G | GRCh38 |
| NC_000023.10:g.154132328A>G , CM000685.1:g.154132328A>G | GRCh37 |
| NC_000023.9:g.153785522A>G | NCBI36 |
| NG_011403.1:g.123671T>C | |
| NG_011403.2:g.123671T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5851T>C MANE Select | ENSP00000353393.4:p.Leu1951= | |
| ENST00000360256.8:c.5851T>C | ENSP00000353393.4:p.Leu1951= | |
| NM_000132.3:c.5851T>C | NP_000123.1:p.Leu1951= | |
| XM_011531126.1:c.5746T>C | XP_011529428.1:p.Leu1916= | |
| NM_000132.4:c.5851T>C MANE Select | NP_000123.1:p.Leu1951= |