Linked Data
dbSNP Id:
rs1172699967
gnomAD v3:
X-155022562-C-T
gnomAD v4:
X-155022562-C-T
MyVariant Identifiers:
chrX:g.155022562C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022562C>T , CM000685.2:g.155022562C>T | GRCh38 |
| NC_000023.10:g.154250837C>T , CM000685.1:g.154250837C>T | GRCh37 |
| NC_000023.9:g.153904031C>T | NCBI36 |
| NG_011403.1:g.5162G>A | |
| NG_011403.2:g.5162G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.-10G>A MANE Select | ENSP00000353393.4:n.-10G>A | |
| ENST00000647125.1:c.-10G>A | ENSP00000496062.1:n.-10G>A | |
| ENST00000360256.8:c.-10G>A | ENSP00000353393.4:n.-10G>A | |
| ENST00000423959.5:c.38+4218G>A | ENSP00000409446.1:n.38+4218G>A | |
| ENST00000453950.1:c.39-66G>A | ENSP00000389153.1:n.39-66G>A | |
| NM_000132.3:c.-10G>A | NP_000123.1:n.-10G>A | |
| XM_011531126.1:c.38+4218G>A | XP_011529428.1:n.38+4218G>A | |
| NM_000132.4:c.-10G>A MANE Select | NP_000123.1:n.-10G>A |