Linked Data
ClinVar Variation Id:
2953126
ClinVar RCV Id:
RCV003810244
MyVariant Identifiers:
chr7:g.143021598C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143324505C>T , CM000669.2:g.143324505C>T | GRCh38 |
| NC_000007.13:g.143021598C>T , CM000669.1:g.143021598C>T | GRCh37 |
| NC_000007.12:g.142731720C>T | NCBI36 |
| NG_009815.1:g.13380C>T | |
| NG_009815.2:g.13380C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650516.2:c.853+608C>T | ENSP00000498052.2:n.853+608C>T | |
| ENST00000343257.7:c.853+13C>T MANE Select | ENSP00000339867.2:n.853+13C>T | |
| ENST00000432192.6:c.677+13C>T | ||
| ENST00000455478.6:c.441+13C>T | ENSP00000400027.2:n.441+13C>T | |
| ENST00000650516.1:c.853+608C>T | ENSP00000498052.1:n.853+608C>T | |
| ENST00000343257.6:c.853+13C>T | ENSP00000339867.2:n.853+13C>T | |
| ENST00000432192.5:c.367+13C>T | ||
| ENST00000455478.5:c.445+13C>T | ||
| ENST00000495612.1:n.154+2657C>T | ||
| NM_000083.2:c.853+13C>T | NP_000074.2:n.853+13C>T | |
| NR_046453.1:n.943+13C>T | ||
| XM_011515781.1:c.853+608C>T | XP_011514083.1:n.853+608C>T | |
| XM_017011739.1:c.403+2657C>T | XP_016867228.1:n.403+2657C>T | |
| XM_017011740.1:c.403+2657C>T | XP_016867229.1:n.403+2657C>T | |
| NM_000083.3:c.853+13C>T MANE Select | NP_000074.3:n.853+13C>T | |
| NR_046453.2:n.958+13C>T |