Linked Data
dbSNP Id:
rs2147089119
gnomAD v4:
X-64192216-C-T
MyVariant Identifiers:
chrX:g.63412096C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64192216C>T , CM000685.2:g.64192216C>T | GRCh38 |
| NC_000023.10:g.63412096C>T , CM000685.1:g.63412096C>T | GRCh37 |
| NC_000023.9:g.63328821C>T | NCBI36 |
| NG_021345.1:g.18529G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374869.8:c.1071G>A MANE Select | ENSP00000364003.4:p.Lys357= | |
| ENST00000330258.3:c.1071G>A | ENSP00000329117.3:p.Lys357= | |
| ENST00000374869.7:c.1071G>A | ENSP00000364003.3:p.Lys357= | |
| NM_152424.3:c.1071G>A | NP_689637.3:p.Lys357= | |
| XM_011530858.1:c.1071G>A | XP_011529160.1:p.Lys357= | |
| NM_152424.4:c.1071G>A MANE Select | NP_689637.3:p.Lys357= |