Linked Data
ClinVar Variation Id:
1929208
ClinVar RCV Id:
RCV002618613
dbSNP Id:
rs1930265020
gnomAD v3:
X-64192221-T-A
gnomAD v4:
X-64192221-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64192221T>A , CM000685.2:g.64192221T>A | GRCh38 |
| NC_000023.10:g.63412101T>A , CM000685.1:g.63412101T>A | GRCh37 |
| NC_000023.9:g.63328826T>A | NCBI36 |
| NG_021345.1:g.18524A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374869.8:c.1066A>T MANE Select | ENSP00000364003.4:p.Thr356Ser | |
| ENST00000330258.3:c.1066A>T | ENSP00000329117.3:p.Thr356Ser | |
| ENST00000374869.7:c.1066A>T | ENSP00000364003.3:p.Thr356Ser | |
| NM_152424.3:c.1066A>T | NP_689637.3:p.Thr356Ser | |
| XM_011530858.1:c.1066A>T | XP_011529160.1:p.Thr356Ser | |
| NM_152424.4:c.1066A>T MANE Select | NP_689637.3:p.Thr356Ser |