Linked Data
dbSNP Id:
rs1369129367
gnomAD v2:
4-4864419-G-T
gnomAD v3:
4-4862692-G-T
gnomAD v4:
4-4862692-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862692G>T , CM000666.2:g.4862692G>T | GRCh38 |
| NC_000004.11:g.4864419G>T , CM000666.1:g.4864419G>T | GRCh37 |
| NC_000004.10:g.4915320G>T | NCBI36 |
| NG_008121.1:g.8028G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.470-9G>T MANE Select | ENSP00000372170.4:n.470-9G>T | |
| ENST00000382723.4:c.470-9G>T | ENSP00000372170.4:n.470-9G>T | |
| ENST00000468421.1:n.182-9G>T | ||
| NM_002448.3:c.470-9G>T MANE Select | NP_002439.2:n.470-9G>T |