Linked Data
dbSNP Id:
rs2073173691
gnomAD v3:
X-154928732-G-A
gnomAD v4:
X-154928732-G-A
MyVariant Identifiers:
chrX:g.154157007G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928732G>A , CM000685.2:g.154928732G>A | GRCh38 |
| NC_000023.10:g.154157007G>A , CM000685.1:g.154157007G>A | GRCh37 |
| NC_000023.9:g.153810201G>A | NCBI36 |
| NG_011403.1:g.98992C>T | |
| NG_011403.2:g.98992C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5058C>T MANE Select | ENSP00000353393.4:p.Thr1686= | |
| ENST00000360256.8:c.5058C>T | ENSP00000353393.4:p.Thr1686= | |
| NM_000132.3:c.5058C>T | NP_000123.1:p.Thr1686= | |
| XM_011531126.1:c.4953C>T | XP_011529428.1:p.Thr1651= | |
| NM_000132.4:c.5058C>T MANE Select | NP_000123.1:p.Thr1686= |