Linked Data
ClinVar Variation Id:
1152103
ClinVar RCV Id:
RCV001493287
dbSNP Id:
rs1029592483
gnomAD v2:
2-233392992-G-C
gnomAD v3:
2-232528282-G-C
gnomAD v4:
2-232528282-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232528282G>C , CM000664.2:g.232528282G>C | GRCh38 |
| NC_000002.11:g.233392992G>C , CM000664.1:g.233392992G>C | GRCh37 |
| NC_000002.10:g.233101236G>C | NCBI36 |
| NG_008028.1:g.7071G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258385.8:c.264G>C MANE Select | ENSP00000258385.3:p.Leu88= | |
| ENST00000258385.7:c.264G>C | ENSP00000258385.3:p.Leu88= | |
| ENST00000412233.5:c.264G>C | ENSP00000398143.1:p.Leu88= | |
| ENST00000441621.6:c.264G>C | ENSP00000408819.2:p.Leu88= | |
| ENST00000446616.1:c.264G>C | ENSP00000410801.1:p.Leu88= | |
| ENST00000449596.5:c.219G>C | ENSP00000404950.1:p.Leu73= | |
| ENST00000543200.5:c.219G>C | ENSP00000438380.1:p.Leu73= | |
| NM_000751.2:c.264G>C | NP_000742.1:p.Leu88= | |
| NM_001256657.1:c.219G>C | NP_001243586.1:p.Leu73= | |
| NM_001311195.1:c.-8G>C | NP_001298124.1:n.-8G>C | |
| NM_001311196.1:c.-8G>C | NP_001298125.1:n.-8G>C | |
| NR_046333.1:c.-4294966976G>C | ||
| NR_046334.1:c.-4294966976G>C | ||
| XM_011510524.1:c.-8G>C | XP_011508826.1:n.-8G>C | |
| XM_011510524.2:c.-8G>C | XP_011508826.1:n.-8G>C | |
| NM_000751.3:c.264G>C MANE Select | NP_000742.1:p.Leu88= | |
| NM_001311195.2:c.-8G>C | NP_001298124.1:n.-8G>C | |
| NM_001311196.2:c.-8G>C | NP_001298125.1:n.-8G>C | |
| NM_001256657.2:c.219G>C | NP_001243586.1:p.Leu73= |