Linked Data
ClinVar Variation Id:
341068
ClinVar RCV Id:
RCV000311027
dbSNP Id:
rs374509697
ExAC:
22:30054165 G / A
gnomAD v2:
22-30054165-G-A
gnomAD v3:
22-29658176-G-A
gnomAD v4:
22-29658176-G-A
COSMIC:
COSN5990740
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29658176G>A , CM000684.2:g.29658176G>A | GRCh38 |
| NC_000022.10:g.30054165G>A , CM000684.1:g.30054165G>A | GRCh37 |
| NC_000022.9:g.28384165G>A | NCBI36 |
| NG_009057.1:g.59621G>A , LRG_511:g.59621G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361166.10:c.600-13G>A | ENSP00000354529.6:n.600-13G>A | |
| ENST00000673312.2:c.*94-13G>A | ENSP00000500186.2:n.*94-13G>A | |
| ENST00000338641.10:c.600-13G>A MANE Select | ENSP00000344666.5:n.600-13G>A | |
| ENST00000361166.9:c.153-13G>A | ENSP00000354529.5:n.153-13G>A | |
| ENST00000672461.1:c.600-13G>A | ENSP00000500919.1:n.600-13G>A | |
| ENST00000672805.1:c.*482-13G>A | ENSP00000500295.1:n.*482-13G>A | |
| ENST00000672896.1:c.600-13G>A | ENSP00000500117.1:n.600-13G>A | |
| ENST00000673312.1:c.619-13G>A | ENSP00000500186.1:n.619-13G>A | |
| ENST00000334961.11:c.351-13G>A | ENSP00000335652.7:n.351-13G>A | |
| ENST00000338641.8:c.600-13G>A | ENSP00000344666.4:n.600-13G>A | |
| ENST00000353887.8:c.351-13G>A | ENSP00000340626.4:n.351-13G>A | |
| ENST00000361166.8:c.600-13G>A | ENSP00000354529.4:n.600-13G>A | |
| ENST00000361452.8:c.477-13G>A | ENSP00000354897.4:n.477-13G>A | |
| ENST00000361676.8:c.474-13G>A | ENSP00000355183.4:n.474-13G>A | |
| ENST00000397789.3:c.600-13G>A | ENSP00000380891.3:n.600-13G>A | |
| ENST00000403435.5:c.600-13G>A | ENSP00000384029.1:n.600-13G>A | |
| ENST00000403999.7:c.600-13G>A | ENSP00000384797.3:n.600-13G>A | |
| ENST00000413209.6:c.447+15891G>A | ENSP00000409921.2:n.447+15891G>A | |
| ENST00000432151.5:c.199-3029G>A | ENSP00000395885.1:n.199-3029G>A | |
| NM_000268.3:c.600-13G>A , LRG_511t1:c.600-13G>A | NP_000259.1:n.600-13G>A | |
| NM_016418.5:c.600-13G>A , LRG_511t2:c.600-13G>A | NP_057502.2:n.600-13G>A | |
| NM_181825.2:c.600-13G>A | NP_861546.1:n.600-13G>A | |
| NM_181828.2:c.474-13G>A | NP_861966.1:n.474-13G>A | |
| NM_181829.2:c.477-13G>A | NP_861967.1:n.477-13G>A | |
| NM_181830.2:c.351-13G>A | NP_861968.1:n.351-13G>A | |
| NM_181831.2:c.351-13G>A | NP_861969.1:n.351-13G>A | |
| NM_181832.2:c.600-13G>A | NP_861970.1:n.600-13G>A | |
| NM_181833.2:c.447+15891G>A | NP_861971.1:n.447+15891G>A | |
| NR_156186.1:n.1159-13G>A | ||
| XM_017028809.2:c.486-13G>A | XP_016884298.1:n.486-13G>A | |
| XM_017028810.1:c.486-13G>A | XP_016884299.1:n.486-13G>A | |
| NM_000268.4:c.600-13G>A MANE Select | NP_000259.1:n.600-13G>A | |
| NM_181825.3:c.600-13G>A | NP_861546.1:n.600-13G>A | |
| NM_181828.3:c.474-13G>A | NP_861966.1:n.474-13G>A | |
| NM_181829.3:c.477-13G>A | NP_861967.1:n.477-13G>A | |
| NM_181830.3:c.351-13G>A | NP_861968.1:n.351-13G>A | |
| NM_181831.3:c.351-13G>A | NP_861969.1:n.351-13G>A | |
| NM_181832.3:c.600-13G>A | NP_861970.1:n.600-13G>A | |
| NR_156186.2:n.1082-13G>A | ||
| NM_181833.3:c.447+15891G>A | NP_861971.1:n.447+15891G>A |