Linked Data
dbSNP Id:
rs1789842651
gnomAD v4:
6-32222521-A-G
MyVariant Identifiers:
chr6:g.32190298A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32222521A>G , CM000668.2:g.32222521A>G | GRCh38 |
| NC_000006.11:g.32190298A>G , CM000668.1:g.32190298A>G | GRCh37 |
| NC_000006.10:g.32298276A>G | NCBI36 |
| NG_028190.1:g.6547T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.441T>C MANE Select | ENSP00000364163.3:p.Pro147= | |
| ENST00000473562.1:n.570T>C | ||
| NM_004557.3:c.441T>C | NP_004548.3:p.Pro147= | |
| NR_134949.1:n.580T>C | ||
| NR_134950.1:n.580T>C | ||
| NM_004557.4:c.441T>C MANE Select | NP_004548.3:p.Pro147= | |
| NR_134949.2:n.580T>C | ||
| NR_134950.2:n.580T>C |