Linked Data
ClinVar Variation Id:
1234710
ClinVar RCV Id:
RCV001621474
dbSNP Id:
rs111502421
gnomAD v2:
11-2799153-T-C
gnomAD v3:
11-2777923-T-C
gnomAD v4:
11-2777923-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2777923T>C , CM000673.2:g.2777923T>C | GRCh38 |
| NC_000011.9:g.2799153T>C , CM000673.1:g.2799153T>C | GRCh37 |
| NC_000011.8:g.2755729T>C | NCBI36 |
| NG_008935.1:g.337933T>C , LRG_287:g.337933T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000496887.7:c.1376-53T>C | ENSP00000434560.2:n.1376-53T>C | |
| ENST00000646564.2:c.1193-53T>C | ENSP00000495806.2:n.1193-53T>C | |
| ENST00000155840.12:c.1733-53T>C MANE Select | ENSP00000155840.2:n.1733-53T>C | |
| ENST00000335475.6:c.1352-53T>C | ENSP00000334497.5:n.1352-53T>C | |
| ENST00000526095.2:c.137-53T>C | ENSP00000494939.1:n.137-53T>C | |
| ENST00000646564.1:c.839-53T>C | ENSP00000495806.1:n.839-53T>C | |
| ENST00000155840.9:c.1733-53T>C | ENSP00000155840.2:n.1733-53T>C | |
| ENST00000335475.5:c.1352-53T>C | ENSP00000334497.5:n.1352-53T>C | |
| ENST00000526095.1:n.240-53T>C | ||
| NM_000218.2:c.1733-53T>C , LRG_287t1:c.1733-53T>C | NP_000209.2:n.1733-53T>C | |
| NM_181798.1:c.1352-53T>C , LRG_287t2:c.1352-53T>C | NP_861463.1:n.1352-53T>C | |
| NM_000218.3:c.1733-53T>C MANE Select | NP_000209.2:n.1733-53T>C |