Linked Data
MyVariant Identifiers:
chr6:g.3225786C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225552C>T , CM000668.2:g.3225552C>T | GRCh38 |
| NC_000006.11:g.3225786C>T , CM000668.1:g.3225786C>T | GRCh37 |
| NC_000006.10:g.3170785C>T | NCBI36 |
| NG_016715.1:g.7183G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.537G>A MANE Select | ENSP00000259818.6:p.Val179= | |
| ENST00000680070.1:n.1467G>A | ||
| ENST00000681707.1:n.1364G>A | ||
| ENST00000681757.1:n.842G>A | ||
| ENST00000259818.7:c.537G>A | ENSP00000259818.6:p.Val179= | |
| ENST00000473006.1:n.654G>A | ||
| NM_178012.4:c.537G>A | NP_821080.1:p.Val179= | |
| XM_011514571.1:c.321G>A | XP_011512873.1:p.Val107= | |
| NM_178012.5:c.537G>A MANE Select | NP_821080.1:p.Val179= |