Linked Data
ClinVar Variation Id:
342509
ClinVar RCV Id:
RCV000340038
dbSNP Id:
rs145137834
gnomAD v2:
3-10195252-C-T
gnomAD v3:
3-10153568-C-T
gnomAD v4:
3-10153568-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10153568C>T , CM000665.2:g.10153568C>T | GRCh38 |
| NC_000003.11:g.10195252C>T , CM000665.1:g.10195252C>T | GRCh37 |
| NC_000003.10:g.10170252C>T | NCBI36 |
| NG_008212.3:g.16934C>T , LRG_322:g.16934C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696153.1:c.*3603C>T | ENSP00000512444.1:n.*3603C>T | |
| ENST00000256474.3:c.*3603C>T MANE Select | ENSP00000256474.3:n.*3603C>T | |
| NM_000551.3:c.*3603C>T , LRG_322t1:c.*3603C>T | NP_000542.1:n.*3603C>T | |
| NM_198156.2:c.*3603C>T | NP_937799.1:n.*3603C>T | |
| NM_001354723.1:c.*3799C>T | NP_001341652.1:n.*3799C>T | |
| NM_000551.4:c.*3603C>T MANE Select | NP_000542.1:n.*3603C>T | |
| NM_001354723.2:c.*3799C>T | NP_001341652.1:n.*3799C>T | |
| NM_198156.3:c.*3603C>T | NP_937799.1:n.*3603C>T |