Linked Data
ClinVar Variation Id:
1568546
ClinVar RCV Id:
RCV002217125
dbSNP Id:
rs2132650909
gnomAD v4:
8-27463180-G-A
MyVariant Identifiers:
chr8:g.27320697G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.27463180G>A , CM000670.2:g.27463180G>A | GRCh38 |
| NC_000008.10:g.27320697G>A , CM000670.1:g.27320697G>A | GRCh37 |
| NC_000008.9:g.27376614G>A | NCBI36 |
| NG_015827.1:g.21117C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000407991.3:c.1263C>T MANE Select | ENSP00000385026.1:p.Asp421= | |
| ENST00000240132.7:c.1218C>T | ENSP00000240132.2:p.Asp406= | |
| ENST00000407991.2:c.1263C>T | ENSP00000385026.1:p.Asp421= | |
| ENST00000520600.1:n.290-1426C>T | ||
| ENST00000520933.7:c.1197C>T | ENSP00000429616.2:p.Asp399= | |
| ENST00000523695.5:c.*665C>T | ENSP00000430612.1:n.*665C>T | |
| NM_000742.3:c.1263C>T | NP_000733.2:p.Asp421= | |
| NM_001282455.1:c.1218C>T | NP_001269384.1:p.Asp406= | |
| XM_005273397.1:c.786C>T | XP_005273454.1:p.Asp262= | |
| XM_006716282.1:c.1263C>T | XP_006716345.1:p.Asp421= | |
| XM_011544388.1:c.1263C>T | XP_011542690.1:p.Asp421= | |
| XM_011544389.1:c.669C>T | XP_011542691.1:p.Asp223= | |
| NM_001347705.1:c.786C>T | NP_001334634.1:p.Asp262= | |
| NM_001347706.1:c.786C>T | NP_001334635.1:p.Asp262= | |
| NM_001347707.1:c.669C>T | NP_001334636.1:p.Asp223= | |
| NM_001347708.1:c.669C>T | NP_001334637.1:p.Asp223= | |
| XM_011544389.2:c.669C>T | XP_011542691.1:p.Asp223= | |
| NM_000742.4:c.1263C>T MANE Select | NP_000733.2:p.Asp421= | |
| NM_001282455.2:c.1218C>T | NP_001269384.1:p.Asp406= | |
| NM_001347705.2:c.786C>T | NP_001334634.1:p.Asp262= | |
| NM_001347706.2:c.786C>T | NP_001334635.1:p.Asp262= | |
| NM_001347707.2:c.669C>T | NP_001334636.1:p.Asp223= | |
| NM_001347708.2:c.669C>T | NP_001334637.1:p.Asp223= |