Linked Data
MyVariant Identifiers:
chr12:g.15131027G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14978093G>A , CM000674.2:g.14978093G>A | GRCh38 |
| NC_000012.11:g.15131027G>A , CM000674.1:g.15131027G>A | GRCh37 |
| NC_000012.10:g.15022294G>A | NCBI36 |
| NG_016859.1:g.10072G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266395.3:c.81G>A MANE Select | ENSP00000266395.2:p.Lys27= | |
| ENST00000266395.2:c.81G>A | ENSP00000266395.2:p.Lys27= | |
| NM_006205.2:c.81G>A | NP_006196.1:p.Lys27= | |
| XR_931376.1:n.175+11394C>T | ||
| XM_017019431.2:c.81G>A | XP_016874920.1:p.Lys27= | |
| XR_931376.2:n.389+11394C>T | ||
| NM_006205.3:c.81G>A MANE Select | NP_006196.1:p.Lys27= |