Linked Data
MyVariant Identifiers:
chr6:g.24291234A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24291006A>T , CM000668.2:g.24291006A>T | GRCh38 |
| NC_000006.11:g.24291234A>T , CM000668.1:g.24291234A>T | GRCh37 |
| NC_000006.10:g.24399213A>T | NCBI36 |
| NG_012829.1:g.72047T>A | |
| NG_012829.2:g.97287T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.630T>A MANE Select | ENSP00000367715.3:p.Val210= | |
| ENST00000378454.7:c.630T>A | ENSP00000367715.3:p.Val210= | |
| NM_001195610.1:c.630T>A | NP_001182539.1:p.Val210= | |
| NM_016356.4:c.630T>A | NP_057440.2:p.Val210= | |
| NM_016356.5:c.630T>A MANE Select | NP_057440.2:p.Val210= | |
| NM_001195610.2:c.630T>A | NP_001182539.1:p.Val210= |