Linked Data
MyVariant Identifiers:
chr6:g.24658803A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24658575A>G , CM000668.2:g.24658575A>G | GRCh38 |
| NC_000006.11:g.24658803A>G , CM000668.1:g.24658803A>G | GRCh37 |
| NC_000006.10:g.24766782A>G | NCBI36 |
| NG_052787.1:g.13313T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378198.9:c.411T>C MANE Select | ENSP00000367440.4:p.Cys137= | |
| ENST00000341060.3:c.237T>C | ENSP00000345345.3:p.Cys79= | |
| ENST00000378198.8:c.411T>C | ENSP00000367440.4:p.Cys137= | |
| ENST00000478285.1:n.598T>C | ||
| ENST00000478507.1:n.320-5422T>C | ||
| NM_016614.2:c.411T>C | NP_057698.2:p.Cys137= | |
| XR_926244.1:n.538T>C | ||
| NM_016614.3:c.411T>C MANE Select | NP_057698.2:p.Cys137= |