Linked Data
MyVariant Identifiers:
chr6:g.24205287C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24205059C>A , CM000668.2:g.24205059C>A | GRCh38 |
| NC_000006.11:g.24205287C>A , CM000668.1:g.24205287C>A | GRCh37 |
| NC_000006.10:g.24313266C>A | NCBI36 |
| NG_012829.1:g.157994G>T | |
| NG_012829.2:g.183234G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.966G>T MANE Select | ENSP00000367715.3:p.Arg322= | |
| ENST00000378450.6:c.225G>T | ENSP00000367711.3:p.Arg75= | |
| ENST00000378454.7:c.966G>T | ENSP00000367715.3:p.Arg322= | |
| NM_001195610.1:c.966G>T | NP_001182539.1:p.Arg322= | |
| NM_016356.4:c.966G>T | NP_057440.2:p.Arg322= | |
| NM_016356.5:c.966G>T MANE Select | NP_057440.2:p.Arg322= | |
| NM_001195610.2:c.966G>T | NP_001182539.1:p.Arg322= |