Linked Data
MyVariant Identifiers:
chr6:g.24146159T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24145931T>A , CM000668.2:g.24145931T>A | GRCh38 |
| NC_000006.11:g.24146159T>A , CM000668.1:g.24146159T>A | GRCh37 |
| NC_000006.10:g.24254138T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378491.9:c.573T>A MANE Select | ENSP00000367752.4:p.Pro191= | |
| ENST00000378478.5:c.573T>A | ENSP00000367739.2:p.Pro191= | |
| ENST00000378491.8:c.573T>A | ENSP00000367752.4:p.Pro191= | |
| ENST00000468195.2:n.257-8840T>A | ||
| NM_080723.4:c.573T>A | NP_542454.3:p.Pro191= | |
| NM_080723.5:c.573T>A MANE Select | NP_542454.3:p.Pro191= |