Linked Data
dbSNP Id:
rs1301798100
gnomAD v4:
X-116173504-C-T
MyVariant Identifiers:
chrX:g.116173504C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116173504C>T , CM000685.2:g.116173504C>T | GRCh38 |
| NC_000023.10:g.115304757C>T , CM000685.1:g.115304757C>T | GRCh37 |
| NC_000023.9:g.115218785C>T | NCBI36 |
| NG_016326.1:g.7800C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.*132C>T MANE Select | ENSP00000360973.4:n.*132C>T | |
| ENST00000371906.4:c.*132C>T | ENSP00000360973.4:n.*132C>T | |
| NM_000686.4:c.*132C>T | NP_000677.2:n.*132C>T | |
| XM_011537533.1:c.*132C>T | XP_011535835.1:n.*132C>T | |
| NM_000686.5:c.*132C>T MANE Select | NP_000677.2:n.*132C>T | |
| NM_001385624.1:c.*132C>T | NP_001372553.1:n.*132C>T |