Linked Data
dbSNP Id:
rs912678541
gnomAD v3:
9-86085066-C-T
gnomAD v4:
9-86085066-C-T
MyVariant Identifiers:
chr9:g.86085066C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.86085066C>T , CM000671.2:g.86085066C>T | GRCh38 |
| NC_000009.11:g.88699981C>T , CM000671.1:g.88699981C>T | GRCh37 |
| NC_000009.10:g.87889801C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000388711.7:c.-21-5725G>A | ENSP00000373363.3:n.-21-5725G>A | |
| ENST00000388712.7:c.-21-5725G>A MANE Select | ENSP00000373364.3:n.-21-5725G>A | |
| ENST00000466178.1:c.-141-27G>A | ENSP00000418155.1:n.-141-27G>A | |
| ENST00000472919.1:n.150-5725G>A | ||
| NM_016548.3:c.-21-5725G>A | NP_057632.2:n.-21-5725G>A | |
| NM_177937.2:c.-21-5725G>A | NP_808800.1:n.-21-5725G>A | |
| NM_016548.4:c.-21-5725G>A MANE Select | NP_057632.2:n.-21-5725G>A | |
| NM_177937.3:c.-21-5725G>A | NP_808800.1:n.-21-5725G>A |