Linked Data
MyVariant Identifiers:
chr6:g.42689989C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42722251C>T , CM000668.2:g.42722251C>T | GRCh38 |
| NC_000006.11:g.42689989C>T , CM000668.1:g.42689989C>T | GRCh37 |
| NC_000006.10:g.42797967C>T | NCBI36 |
| NG_009176.1:g.5370G>A | |
| NG_009176.2:g.5370G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.84G>A MANE Select | ENSP00000230381.5:p.Val28= | |
| ENST00000230381.6:c.84G>A | ENSP00000230381.5:p.Val28= | |
| NM_000322.4:c.84G>A | NP_000313.2:p.Val28= | |
| XR_427834.2:n.739G>A | ||
| XR_926295.1:n.739G>A | ||
| XR_427834.4:n.789G>A | ||
| XR_926295.3:n.789G>A | ||
| NM_000322.5:c.84G>A MANE Select | NP_000313.2:p.Val28= |