Linked Data
MyVariant Identifiers:
chr12:g.52845323C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52451539C>T , CM000674.2:g.52451539C>T | GRCh38 |
| NC_000012.11:g.52845323C>T , CM000674.1:g.52845323C>T | GRCh37 |
| NC_000012.10:g.51131590C>T | NCBI36 |
| NG_008299.1:g.5588G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252252.4:c.540G>A MANE Select | ENSP00000252252.3:p.Lys180= | |
| ENST00000252252.3:c.540G>A | ENSP00000252252.3:p.Lys180= | |
| NM_005555.3:c.540G>A | NP_005546.2:p.Lys180= | |
| NM_005555.4:c.540G>A MANE Select | NP_005546.2:p.Lys180= |