Linked Data
MyVariant Identifiers:
chr6:g.32411552T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443775T>A , CM000668.2:g.32443775T>A | GRCh38 |
| NC_000006.11:g.32411552T>A , CM000668.1:g.32411552T>A | GRCh37 |
| NC_000006.10:g.32519530T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000395388.7:c.630T>A MANE Select | ENSP00000378786.2:p.Pro210= | |
| ENST00000374982.5:c.555T>A | ENSP00000364121.5:p.Pro185= | |
| ENST00000395388.6:c.630T>A | ENSP00000378786.2:p.Pro210= | |
| NM_019111.4:c.630T>A | NP_061984.2:p.Pro210= | |
| NM_019111.5:c.630T>A MANE Select | NP_061984.2:p.Pro210= |