Linked Data
MyVariant Identifiers:
chr6:g.3226032G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225798G>T , CM000668.2:g.3225798G>T | GRCh38 |
| NC_000006.11:g.3226032G>T , CM000668.1:g.3226032G>T | GRCh37 |
| NC_000006.10:g.3171031G>T | NCBI36 |
| NG_016715.1:g.6937C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.291C>A MANE Select | ENSP00000259818.6:p.Ala97= | |
| ENST00000680070.1:n.1221C>A | ||
| ENST00000681707.1:n.1118C>A | ||
| ENST00000681757.1:n.596C>A | ||
| ENST00000259818.7:c.291C>A | ENSP00000259818.6:p.Ala97= | |
| ENST00000473006.1:n.408C>A | ||
| NM_178012.4:c.291C>A | NP_821080.1:p.Ala97= | |
| XM_011514571.1:c.75C>A | XP_011512873.1:p.Ala25= | |
| NM_178012.5:c.291C>A MANE Select | NP_821080.1:p.Ala97= |