Linked Data
ClinVar Variation Id:
2129433
ClinVar RCV Id:
RCV003040536
gnomAD v4:
10-100989215-A-G
MyVariant Identifiers:
chr10:g.102748972A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100989215A>G , CM000672.2:g.100989215A>G | GRCh38 |
| NC_000010.10:g.102748972A>G , CM000672.1:g.102748972A>G | GRCh37 |
| NC_000010.9:g.102738962A>G | NCBI36 |
| NG_011646.1:g.3301T>C | |
| NG_012624.1:g.6680A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311916.8:c.1005A>G MANE Select | ENSP00000309595.2:p.Pro335= | |
| ENST00000370228.2:c.1005A>G | ENSP00000359248.1:p.Pro335= | |
| ENST00000643860.1:c.1005A>G | ENSP00000494389.1:p.Pro335= | |
| ENST00000646226.1:n.59-429A>G | ||
| ENST00000650396.1:c.28A>G | ||
| ENST00000311916.6:c.1005A>G | ENSP00000309595.2:p.Pro335= | |
| ENST00000370228.1:c.1005A>G | ENSP00000359248.1:p.Pro335= | |
| ENST00000459764.1:n.87-429A>G | ||
| ENST00000473656.5:n.65-429A>G | ||
| ENST00000476766.5:n.192-491A>G | ||
| NM_001163812.1:c.1005A>G | NP_001157284.1:p.Pro335= | |
| NM_001163813.1:c.-119-429A>G | NP_001157285.1:n.-119-429A>G | |
| NM_001163814.1:c.-119-429A>G | NP_001157286.1:n.-119-429A>G | |
| NM_021830.4:c.1005A>G | NP_068602.2:p.Pro335= | |
| XM_011539975.1:c.-57-491A>G | XP_011538277.1:n.-57-491A>G | |
| XR_945788.1:n.1838A>G | ||
| XM_011539975.2:c.-57-491A>G | XP_011538277.1:n.-57-491A>G | |
| XM_017016437.1:c.-296A>G | XP_016871926.1:n.-296A>G | |
| XR_001747142.1:n.1179A>G | ||
| XR_001747144.1:n.1179A>G | ||
| XR_002956991.1:n.1179A>G | ||
| XR_945788.2:n.1179A>G | ||
| NM_021830.5:c.1005A>G MANE Select | NP_068602.2:p.Pro335= | |
| NM_001163812.2:c.1005A>G | NP_001157284.1:p.Pro335= | |
| NM_001163813.2:c.-119-429A>G | NP_001157285.1:n.-119-429A>G | |
| NM_001163814.2:c.-119-429A>G | NP_001157286.1:n.-119-429A>G | |
| NM_001368275.1:c.-57-491A>G | NP_001355204.1:n.-57-491A>G | |
| NR_160738.1:n.1673A>G | ||
| NR_160739.1:n.72-429A>G | ||
| NR_160740.1:n.1673A>G | ||
| NR_160741.1:n.1673A>G | ||
| NR_160742.1:n.1673A>G |