Linked Data
MyVariant Identifiers:
chr6:g.42689725A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721987A>T , CM000668.2:g.42721987A>T | GRCh38 |
| NC_000006.11:g.42689725A>T , CM000668.1:g.42689725A>T | GRCh37 |
| NC_000006.10:g.42797703A>T | NCBI36 |
| NG_009176.1:g.5634T>A | |
| NG_009176.2:g.5634T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.348T>A MANE Select | ENSP00000230381.5:p.Ala116= | |
| ENST00000230381.6:c.348T>A | ENSP00000230381.5:p.Ala116= | |
| NM_000322.4:c.348T>A | NP_000313.2:p.Ala116= | |
| XR_427834.2:n.1003T>A | ||
| XR_926295.1:n.1003T>A | ||
| XR_427834.4:n.1053T>A | ||
| XR_926295.3:n.1053T>A | ||
| NM_000322.5:c.348T>A MANE Select | NP_000313.2:p.Ala116= |