Linked Data
ClinVar Variation Id:
1286334
ClinVar RCV Id:
RCV001710116
dbSNP Id:
rs11912763
ExAC:
22:36684722 G / A
gnomAD v2:
22-36684722-G-A
gnomAD v3:
22-36288676-G-A
gnomAD v4:
22-36288676-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36288676G>A , CM000684.2:g.36288676G>A | GRCh38 |
| NC_000022.10:g.36684722G>A , CM000684.1:g.36684722G>A | GRCh37 |
| NC_000022.9:g.35014668G>A | NCBI36 |
| NG_011884.2:g.104343C>T , LRG_567:g.104343C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000685801.1:c.4833+51C>T | ENSP00000510688.1:n.4833+51C>T | |
| ENST00000691109.1:n.5065+51C>T | ||
| ENST00000216181.11:c.4770+51C>T MANE Select | ENSP00000216181.6:n.4770+51C>T | |
| ENST00000216181.9:c.4770+51C>T | ENSP00000216181.5:n.4770+51C>T | |
| NM_002473.5:c.4770+51C>T , LRG_567t1:c.4770+51C>T | NP_002464.1:n.4770+51C>T | |
| XM_011530197.1:c.4770+51C>T | XP_011528499.1:n.4770+51C>T | |
| XM_011530197.2:c.4770+51C>T | XP_011528499.1:n.4770+51C>T | |
| XM_017028803.1:c.4770+51C>T | XP_016884292.1:n.4770+51C>T | |
| XM_017028804.1:c.4770+51C>T | XP_016884293.1:n.4770+51C>T | |
| XM_017028805.1:c.4770+51C>T | XP_016884294.1:n.4770+51C>T | |
| XM_017028806.1:c.4770+51C>T | XP_016884295.1:n.4770+51C>T | |
| NM_002473.6:c.4770+51C>T MANE Select | NP_002464.1:n.4770+51C>T |