Linked Data
ClinVar Variation Id:
211265
dbSNP Id:
rs757442837
ExAC:
X:73960755 C / T
gnomAD v2:
X-73960755-C-T
gnomAD v3:
X-74740920-C-T
gnomAD v4:
X-74740920-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74740920C>T , CM000685.2:g.74740920C>T | GRCh38 |
| NC_000023.10:g.73960755C>T , CM000685.1:g.73960755C>T | GRCh37 |
| NC_000023.9:g.73877480C>T | NCBI36 |
| NG_027726.1:g.189533G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000055682.12:c.3637G>A MANE Select | ENSP00000055682.5:p.Gly1213Ser | |
| ENST00000616200.2:c.3637G>A | ENSP00000480284.1:p.Gly1213Ser | |
| ENST00000642681.2:c.3637G>A | ENSP00000495800.1:p.Gly1213Ser | |
| ENST00000055682.10:c.3637G>A | ENSP00000055682.5:p.Gly1213Ser | |
| ENST00000616200.1:c.3637G>A | ENSP00000480284.1:p.Gly1213Ser | |
| NM_001008537.2:c.3637G>A | NP_001008537.1:p.Gly1213Ser | |
| XM_011530935.1:c.3637G>A | XP_011529237.1:p.Gly1213Ser | |
| NM_001008537.3:c.3637G>A MANE Select | NP_001008537.1:p.Gly1213Ser |