Linked Data
dbSNP Id:
rs1557180317
gnomAD v2:
X-153599640-G-A
gnomAD v4:
X-154371272-G-A
MyVariant Identifiers:
chrX:g.153599640G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154371272G>A , CM000685.2:g.154371272G>A | GRCh38 |
| NC_000023.10:g.153599640G>A , CM000685.1:g.153599640G>A | GRCh37 |
| NC_000023.9:g.153252834G>A | NCBI36 |
| NG_008677.1:g.1845G>A , LRG_745:g.1845G>A | |
| NG_011506.1:g.8367C>T | |
| NG_011506.2:g.8367C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.-27C>T | ENSP00000353467.4:n.-27C>T | |
| ENST00000369850.10:c.-27C>T MANE Select | ENSP00000358866.3:n.-27C>T | |
| ENST00000422373.6:c.-27C>T | ENSP00000416926.2:n.-27C>T | |
| ENST00000344736.8:c.-27C>T | ENSP00000358863.3:n.-27C>T | |
| ENST00000360319.8:c.-27C>T | ENSP00000353467.4:n.-27C>T | |
| ENST00000369850.7:c.-27C>T | ENSP00000358866.3:n.-27C>T | |
| ENST00000422373.5:c.-27C>T | ENSP00000416926.1:n.-27C>T | |
| ENST00000610817.4:c.-108C>T | ENSP00000480593.1:n.-108C>T | |
| NM_001110556.1:c.-27C>T | NP_001104026.1:n.-27C>T | |
| NM_001456.3:c.-27C>T | NP_001447.2:n.-27C>T | |
| XM_011531127.1:c.-27C>T | XP_011529429.1:n.-27C>T | |
| XM_011531128.1:c.-27C>T | XP_011529430.1:n.-27C>T | |
| XM_011531129.1:c.-27C>T | XP_011529431.1:n.-27C>T | |
| XM_011531130.1:c.-27C>T | XP_011529432.1:n.-27C>T | |
| XM_011531131.1:c.-27C>T | XP_011529433.1:n.-27C>T | |
| NM_001110556.2:c.-27C>T MANE Select | NP_001104026.1:n.-27C>T | |
| NM_001456.4:c.-27C>T | NP_001447.2:n.-27C>T |