Linked Data
dbSNP Id:
rs941763995
gnomAD v4:
X-78123092-T-A
MyVariant Identifiers:
chrX:g.78123092T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78123092T>A , CM000685.2:g.78123092T>A | GRCh38 |
| NC_000023.10:g.77378589T>A , CM000685.1:g.77378589T>A | GRCh37 |
| NC_000023.9:g.77265245T>A | NCBI36 |
| NG_008862.1:g.23924T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.757-103T>A MANE Select | ENSP00000362413.4:n.757-103T>A | |
| ENST00000644362.1:c.673-103T>A | ENSP00000496140.1:n.673-103T>A | |
| ENST00000373316.4:c.757-103T>A | ENSP00000362413.4:n.757-103T>A | |
| ENST00000474281.1:n.163+91T>A | ||
| NM_000291.3:c.757-103T>A | NP_000282.1:n.757-103T>A | |
| NM_000291.4:c.757-103T>A MANE Select | NP_000282.1:n.757-103T>A |