Linked Data
ClinVar Variation Id:
507919
dbSNP Id:
rs764817290
ExAC:
9:137726990 C / T
gnomAD v2:
9-137726990-C-T
gnomAD v3:
9-134835144-C-T
gnomAD v4:
9-134835144-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134835144C>T , CM000671.2:g.134835144C>T | GRCh38 |
| NC_000009.11:g.137726990C>T , CM000671.1:g.137726990C>T | GRCh37 |
| NC_000009.10:g.136866811C>T | NCBI36 |
| NG_008030.1:g.198339C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.5310C>T | ENSP00000360885.4:p.Asn1770= | |
| ENST00000371817.8:c.5310C>T MANE Select | ENSP00000360882.3:p.Asn1770= | |
| ENST00000371817.7:c.5310C>T | ENSP00000360882.3:p.Asn1770= | |
| ENST00000371820.3:c.568C>T | ||
| ENST00000618395.4:c.5310C>T | ENSP00000481360.1:p.Asn1770= | |
| NM_000093.4:c.5310C>T | NP_000084.3:p.Asn1770= | |
| NM_001278074.1:c.5310C>T | NP_001265003.1:p.Asn1770= | |
| NR_103451.2:n.71-14935G>A | ||
| NM_000093.5:c.5310C>T MANE Select | NP_000084.3:p.Asn1770= |