Linked Data
ClinVar Variation Id:
2929561
ClinVar RCV Id:
RCV003784727
dbSNP Id:
rs1602179326
gnomAD v3:
X-48688790-A-C
gnomAD v4:
X-48688790-A-C
MyVariant Identifiers:
chrX:g.48547179A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48688790A>C , CM000685.2:g.48688790A>C | GRCh38 |
| NC_000023.10:g.48547179A>C , CM000685.1:g.48547179A>C | GRCh37 |
| NC_000023.9:g.48432123A>C | NCBI36 |
| NG_007877.1:g.9994A>C , LRG_125:g.9994A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474174.2:n.306A>C | ||
| ENST00000698625.1:c.1062A>C | ENSP00000513844.1:p.Pro354= | |
| ENST00000698626.1:c.1062A>C | ENSP00000513845.1:p.Pro354= | |
| ENST00000698635.1:c.1062A>C | ENSP00000513850.1:p.Pro354= | |
| ENST00000376701.5:c.1062A>C MANE Select | ENSP00000365891.4:p.Pro354= | |
| ENST00000376701.4:c.1062A>C | ENSP00000365891.4:p.Pro354= | |
| ENST00000474174.1:n.306A>C | ||
| NM_000377.2:c.1062A>C , LRG_125t1:c.1062A>C | NP_000368.1:p.Pro354= | |
| XM_011543977.1:c.932-26A>C | XP_011542279.1:n.932-26A>C | |
| XM_011543977.2:c.932-26A>C | XP_011542279.1:n.932-26A>C | |
| XM_017029786.1:c.1062A>C | XP_016885275.1:p.Pro354= | |
| NM_000377.3:c.1062A>C MANE Select | NP_000368.1:p.Pro354= |