Linked Data
ClinVar Variation Id:
754760
ClinVar RCV Id:
RCV003594060
dbSNP Id:
rs1564187943
gnomAD v4:
9-134835129-C-T
MyVariant Identifiers:
chr9:g.137726975C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134835129C>T , CM000671.2:g.134835129C>T | GRCh38 |
| NC_000009.11:g.137726975C>T , CM000671.1:g.137726975C>T | GRCh37 |
| NC_000009.10:g.136866796C>T | NCBI36 |
| NG_008030.1:g.198324C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.5295C>T | ENSP00000360885.4:p.Arg1765= | |
| ENST00000371817.8:c.5295C>T MANE Select | ENSP00000360882.3:p.Arg1765= | |
| ENST00000371817.7:c.5295C>T | ENSP00000360882.3:p.Arg1765= | |
| ENST00000371820.3:c.553C>T | ||
| ENST00000618395.4:c.5295C>T | ENSP00000481360.1:p.Arg1765= | |
| NM_000093.4:c.5295C>T | NP_000084.3:p.Arg1765= | |
| NM_001278074.1:c.5295C>T | NP_001265003.1:p.Arg1765= | |
| NR_103451.2:n.71-14920G>A | ||
| NM_000093.5:c.5295C>T MANE Select | NP_000084.3:p.Arg1765= |