Linked Data
MyVariant Identifiers:
chr12:g.6145586A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6036420A>T , CM000674.2:g.6036420A>T | GRCh38 |
| NC_000012.11:g.6145586A>T , CM000674.1:g.6145586A>T | GRCh37 |
| NC_000012.10:g.6015847A>T | NCBI36 |
| NG_009072.1:g.93251T>A | |
| NG_009072.2:g.93251T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.2514T>A MANE Select | ENSP00000261405.5:p.Pro838= | |
| ENST00000261405.9:c.2514T>A | ENSP00000261405.5:p.Pro838= | |
| ENST00000538635.5:n.421-42486T>A | ||
| NM_000552.3:c.2514T>A | NP_000543.2:p.Pro838= | |
| NM_000552.4:c.2514T>A | NP_000543.2:p.Pro838= | |
| NM_000552.5:c.2514T>A MANE Select | NP_000543.3:p.Pro838= |