Linked Data
ClinVar Variation Id:
477628
ClinVar RCV Id:
RCV002060369
dbSNP Id:
rs899378635
gnomAD v3:
4-88007811-G-T
gnomAD v4:
4-88007811-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88007811G>T , CM000666.2:g.88007811G>T | GRCh38 |
| NC_000004.11:g.88928963G>T , CM000666.1:g.88928963G>T | GRCh37 |
| NC_000004.10:g.89147987G>T | NCBI36 |
| NG_008604.1:g.5144G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.78G>T MANE Select | ENSP00000237596.2:p.Pro26= | |
| ENST00000237596.6:c.78G>T | ENSP00000237596.2:p.Pro26= | |
| NM_000297.3:c.78G>T | NP_000288.1:p.Pro26= | |
| XM_011532028.1:c.78G>T | XP_011530330.1:p.Pro26= | |
| XR_244632.2:n.173G>T | ||
| NR_156488.1:n.165G>T | ||
| XM_011532028.2:c.78G>T | XP_011530330.1:p.Pro26= | |
| NM_000297.4:c.78G>T MANE Select | NP_000288.1:p.Pro26= | |
| NR_156488.2:n.177G>T |