Linked Data
ClinVar Variation Id:
2923796
ClinVar RCV Id:
RCV003783354
dbSNP Id:
rs2147316183
MyVariant Identifiers:
chrX:g.66765384C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.67545542C>T , CM000685.2:g.67545542C>T | GRCh38 |
| NC_000023.10:g.66765384C>T , CM000685.1:g.66765384C>T | GRCh37 |
| NC_000023.9:g.66682109C>T | NCBI36 |
| NG_009014.2:g.6511C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396043.4:c.396C>T | ENSP00000379358.4:p.Val132= | |
| ENST00000374690.9:c.396C>T MANE Select | ENSP00000363822.3:p.Val132= | |
| ENST00000396044.8:c.396C>T | ENSP00000379359.3:p.Val132= | |
| ENST00000612452.5:c.396C>T | ENSP00000484033.2:p.Val132= | |
| ENST00000374690.7:c.396C>T | ENSP00000363822.3:p.Val132= | |
| ENST00000396044.7:c.396C>T | ENSP00000379359.3:p.Val132= | |
| ENST00000504326.5:c.396C>T | ENSP00000421155.1:p.Val132= | |
| ENST00000513847.5:n.723C>T | ||
| ENST00000514029.5:c.396C>T | ENSP00000425199.1:p.Val132= | |
| ENST00000612010.4:c.396C>T | ENSP00000482407.1:p.Val132= | |
| ENST00000612452.4:c.-175C>T | ENSP00000484033.1:n.-175C>T | |
| ENST00000613054.2:c.396C>T | ENSP00000479013.1:p.Val132= | |
| NM_000044.3:c.396C>T | NP_000035.2:p.Val132= | |
| NM_000044.4:c.396C>T | NP_000035.2:p.Val132= | |
| NM_001011645.3:c.-1388C>T | NP_001011645.1:n.-1388C>T | |
| NM_001348061.1:c.396C>T | NP_001334990.1:p.Val132= | |
| NM_001348063.1:c.396C>T | NP_001334992.1:p.Val132= | |
| NM_001348064.1:c.396C>T | NP_001334993.1:p.Val132= | |
| NM_000044.6:c.396C>T MANE Select | NP_000035.2:p.Val132= |