Linked Data
ClinVar Variation Id:
2876368
ClinVar RCV Id:
RCV003710236
dbSNP Id:
rs1224664451
gnomAD v2:
17-45360709-C-T
gnomAD v4:
17-47283343-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47283343C>T , CM000679.2:g.47283343C>T | GRCh38 |
| NC_000017.10:g.45360709C>T , CM000679.1:g.45360709C>T | GRCh37 |
| NC_000017.9:g.42715708C>T | NCBI36 |
| NG_008332.2:g.34502C>T , LRG_481:g.34502C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.166-11C>T | ENSP00000513002.1:n.166-11C>T | |
| ENST00000559488.7:c.166-11C>T MANE Select | ENSP00000452786.2:n.166-11C>T | |
| ENST00000559488.5:c.166-11C>T | ENSP00000452786.1:n.166-11C>T | |
| ENST00000560629.1:c.131-11C>T | ||
| ENST00000571680.1:c.166-11C>T | ENSP00000461626.1:n.166-11C>T | |
| NM_000212.2:c.166-11C>T , LRG_481t1:c.166-11C>T | NP_000203.2:n.166-11C>T | |
| NM_000212.3:c.166-11C>T MANE Select | NP_000203.2:n.166-11C>T |