Linked Data
dbSNP Id:
rs1008731705
gnomAD v4:
X-116172112-A-G
MyVariant Identifiers:
chrX:g.116172112A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172112A>G , CM000685.2:g.116172112A>G | GRCh38 |
| NC_000023.10:g.115303365A>G , CM000685.1:g.115303365A>G | GRCh37 |
| NC_000023.9:g.115217393A>G | NCBI36 |
| NG_016326.1:g.6408A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.-35-134A>G MANE Select | ENSP00000360973.4:n.-35-134A>G | |
| ENST00000680409.1:n.300A>G | ||
| ENST00000681852.1:c.-35-134A>G | ENSP00000505750.1:n.-35-134A>G | |
| ENST00000371906.4:c.-35-134A>G | ENSP00000360973.4:n.-35-134A>G | |
| NM_000686.4:c.-35-134A>G | NP_000677.2:n.-35-134A>G | |
| XM_011537533.1:c.-35-134A>G | XP_011535835.1:n.-35-134A>G | |
| NM_000686.5:c.-35-134A>G MANE Select | NP_000677.2:n.-35-134A>G | |
| NM_001385624.1:c.-35-134A>G | NP_001372553.1:n.-35-134A>G |