Linked Data
ClinVar Variation Id:
509955
ClinVar RCV Id:
RCV002529579
dbSNP Id:
rs780810190
ExAC:
4:1803274 C / T
gnomAD v2:
4-1803274-C-T
gnomAD v3:
4-1801547-C-T
gnomAD v4:
4-1801547-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1801547C>T , CM000666.2:g.1801547C>T | GRCh38 |
| NC_000004.11:g.1803274C>T , CM000666.1:g.1803274C>T | GRCh37 |
| NC_000004.10:g.1773072C>T | NCBI36 |
| NG_012632.1:g.13236C>T , LRG_1021:g.13236C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000340107.9:c.615+11C>T | ENSP00000339824.4:n.615+11C>T | |
| ENST00000260795.8:c.615+11C>T | ENSP00000260795.3:n.615+11C>T | |
| ENST00000352904.6:c.615+11C>T | ENSP00000231803.1:n.615+11C>T | |
| ENST00000412135.7:c.603+11C>T | ENSP00000412903.3:n.603+11C>T | |
| ENST00000440486.8:c.615+11C>T MANE Select | ENSP00000414914.2:n.615+11C>T | |
| ENST00000481110.7:c.615+11C>T | ENSP00000420533.2:n.615+11C>T | |
| ENST00000260795.6:c.615+11C>T | ENSP00000260795.2:n.615+11C>T | |
| ENST00000340107.8:c.615+11C>T | ENSP00000339824.4:n.615+11C>T | |
| ENST00000352904.5:c.615+11C>T | ENSP00000231803.1:n.615+11C>T | |
| ENST00000412135.6:c.615+11C>T | ENSP00000412903.2:n.615+11C>T | |
| ENST00000440486.6:c.615+11C>T | ENSP00000414914.2:n.615+11C>T | |
| ENST00000481110.6:c.615+11C>T | ENSP00000420533.2:n.615+11C>T | |
| ENST00000507588.1:c.75+11C>T | ENSP00000427289.1:n.75+11C>T | |
| ENST00000613647.4:c.615+11C>T | ENSP00000479472.1:n.615+11C>T | |
| NM_000142.4:c.615+11C>T , LRG_1021t1:c.615+11C>T | NP_000133.1:n.615+11C>T | |
| NM_001163213.1:c.615+11C>T , LRG_1021t2:c.615+11C>T | NP_001156685.1:n.615+11C>T | |
| NM_022965.3:c.615+11C>T | NP_075254.1:n.615+11C>T | |
| XM_006713868.1:c.615+11C>T | XP_006713931.1:n.615+11C>T | |
| XM_006713869.1:c.615+11C>T | XP_006713932.1:n.615+11C>T | |
| XM_006713870.1:c.615+11C>T | XP_006713933.1:n.615+11C>T | |
| XM_006713871.1:c.615+11C>T | XP_006713934.1:n.615+11C>T | |
| XM_006713872.1:c.615+11C>T | XP_006713935.1:n.615+11C>T | |
| XM_006713873.1:c.615+11C>T | XP_006713936.1:n.615+11C>T | |
| XM_011513420.1:c.615+11C>T | XP_011511722.1:n.615+11C>T | |
| XM_011513422.1:c.615+11C>T | XP_011511724.1:n.615+11C>T | |
| NM_001354809.1:c.615+11C>T | NP_001341738.1:n.615+11C>T | |
| NM_001354810.1:c.615+11C>T | NP_001341739.1:n.615+11C>T | |
| NR_148971.1:n.871+11C>T | ||
| NM_001354809.2:c.615+11C>T | NP_001341738.1:n.615+11C>T | |
| NM_001354810.2:c.615+11C>T | NP_001341739.1:n.615+11C>T | |
| NR_148971.2:n.890+11C>T | ||
| NM_000142.5:c.615+11C>T MANE Select | NP_000133.1:n.615+11C>T | |
| NM_001163213.2:c.615+11C>T | NP_001156685.1:n.615+11C>T | |
| NM_022965.4:c.615+11C>T | NP_075254.1:n.615+11C>T |