Linked Data
MyVariant Identifiers:
chr6:g.24291219A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24290991A>G , CM000668.2:g.24290991A>G | GRCh38 |
| NC_000006.11:g.24291219A>G , CM000668.1:g.24291219A>G | GRCh37 |
| NC_000006.10:g.24399198A>G | NCBI36 |
| NG_012829.1:g.72062T>C | |
| NG_012829.2:g.97302T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.645T>C MANE Select | ENSP00000367715.3:p.Phe215= | |
| ENST00000378454.7:c.645T>C | ENSP00000367715.3:p.Phe215= | |
| NM_001195610.1:c.645T>C | NP_001182539.1:p.Phe215= | |
| NM_016356.4:c.645T>C | NP_057440.2:p.Phe215= | |
| NM_016356.5:c.645T>C MANE Select | NP_057440.2:p.Phe215= | |
| NM_001195610.2:c.645T>C | NP_001182539.1:p.Phe215= |