Linked Data
MyVariant Identifiers:
chr6:g.42689596C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721858C>A , CM000668.2:g.42721858C>A | GRCh38 |
| NC_000006.11:g.42689596C>A , CM000668.1:g.42689596C>A | GRCh37 |
| NC_000006.10:g.42797574C>A | NCBI36 |
| NG_009176.1:g.5763G>T | |
| NG_009176.2:g.5763G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.477G>T MANE Select | ENSP00000230381.5:p.Leu159= | |
| ENST00000230381.6:c.477G>T | ENSP00000230381.5:p.Leu159= | |
| NM_000322.4:c.477G>T | NP_000313.2:p.Leu159= | |
| XR_427834.2:n.1132G>T | ||
| XR_926295.1:n.1132G>T | ||
| XR_427834.4:n.1182G>T | ||
| XR_926295.3:n.1182G>T | ||
| NM_000322.5:c.477G>T MANE Select | NP_000313.2:p.Leu159= |