Linked Data
dbSNP Id:
rs531822319
gnomAD v2:
8-19813300-C-T
gnomAD v3:
8-19955789-C-T
gnomAD v4:
8-19955789-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955789C>T , CM000670.2:g.19955789C>T | GRCh38 |
| NC_000008.10:g.19813300C>T , CM000670.1:g.19813300C>T | GRCh37 |
| NC_000008.9:g.19857580C>T | NCBI36 |
| NG_008855.1:g.21719C>T | |
| NG_008855.2:g.59073C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.776-52C>T MANE Select | ENSP00000497642.1:n.776-52C>T | |
| ENST00000311322.8:c.776-52C>T | ENSP00000309757.6:n.776-52C>T | |
| NM_000237.2:c.776-52C>T | NP_000228.1:n.776-52C>T | |
| NM_000237.3:c.776-52C>T MANE Select | NP_000228.1:n.776-52C>T |