Linked Data
dbSNP Id:
rs982084803
gnomAD v3:
9-33025585-C-T
gnomAD v4:
9-33025585-C-T
MyVariant Identifiers:
chr9:g.33025585C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.33025585C>T , CM000671.2:g.33025585C>T | GRCh38 |
| NC_000009.11:g.33025583C>T , CM000671.1:g.33025583C>T | GRCh37 |
| NC_000009.10:g.33015583C>T | NCBI36 |
| NG_012821.2:g.4547G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330899.5:c.-11+202C>T MANE Select | ENSP00000369127.3:n.-11+202C>T | |
| ENST00000330899.4:c.-11+202C>T | ENSP00000369127.3:n.-11+202C>T | |
| ENST00000495015.5:n.98+202C>T | ||
| NM_001314039.1:c.-304+202C>T | NP_001300968.1:n.-304+202C>T | |
| NM_001539.2:c.-11+202C>T | NP_001530.1:n.-11+202C>T | |
| NM_001539.3:c.-11+202C>T | NP_001530.1:n.-11+202C>T | |
| NM_001539.4:c.-11+202C>T MANE Select | NP_001530.1:n.-11+202C>T | |
| NM_001314039.2:c.-304+202C>T | NP_001300968.1:n.-304+202C>T |