Linked Data
MyVariant Identifiers:
chr6:g.143806310T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143485173T>A , CM000668.2:g.143485173T>A | GRCh38 |
| NC_000006.11:g.143806310T>A , CM000668.1:g.143806310T>A | GRCh37 |
| NC_000006.10:g.143848003T>A | NCBI36 |
| NG_008459.1:g.39393T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367591.5:c.963T>A MANE Select | ENSP00000356563.4:p.Pro321= | |
| ENST00000367591.4:c.963T>A | ENSP00000356563.4:p.Pro321= | |
| ENST00000585848.1:n.102T>A | ||
| NM_003630.2:c.963T>A | NP_003621.1:p.Pro321= | |
| NM_003630.3:c.963T>A MANE Select | NP_003621.1:p.Pro321= |