Linked Data
MyVariant Identifiers:
chr12:g.15131003A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14978069A>C , CM000674.2:g.14978069A>C | GRCh38 |
| NC_000012.11:g.15131003A>C , CM000674.1:g.15131003A>C | GRCh37 |
| NC_000012.10:g.15022270A>C | NCBI36 |
| NG_016859.1:g.10048A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266395.3:c.57A>C MANE Select | ENSP00000266395.2:p.Pro19= | |
| ENST00000266395.2:c.57A>C | ENSP00000266395.2:p.Pro19= | |
| NM_006205.2:c.57A>C | NP_006196.1:p.Pro19= | |
| XR_931376.1:n.175+11418T>G | ||
| XM_017019431.2:c.57A>C | XP_016874920.1:p.Pro19= | |
| XR_931376.2:n.389+11418T>G | ||
| NM_006205.3:c.57A>C MANE Select | NP_006196.1:p.Pro19= |