Linked Data
dbSNP Id:
rs1762604461
gnomAD v3:
6-3154814-A-G
gnomAD v4:
6-3154814-A-G
MyVariant Identifiers:
chr6:g.3155048A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154814A>G , CM000668.2:g.3154814A>G | GRCh38 |
| NC_000006.11:g.3155048A>G , CM000668.1:g.3155048A>G | GRCh37 |
| NC_000006.10:g.3100047A>G | NCBI36 |
| NG_042223.1:g.7736T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.387T>C MANE Select | ENSP00000369703.2:p.Cys129= | |
| ENST00000679400.1:n.443T>C | ||
| ENST00000679907.1:n.775T>C | ||
| ENST00000680036.1:n.1169T>C | ||
| ENST00000680967.1:n.1477T>C | ||
| ENST00000333628.3:c.387T>C | ENSP00000369703.2:p.Cys129= | |
| ENST00000489942.1:n.582T>C | ||
| NM_001069.2:c.387T>C | NP_001060.1:p.Cys129= | |
| NM_001310315.1:c.132T>C | NP_001297244.1:p.Cys44= | |
| NM_001069.3:c.387T>C MANE Select | NP_001060.1:p.Cys129= | |
| NM_001310315.2:c.132T>C | NP_001297244.1:p.Cys44= |