Linked Data
MyVariant Identifiers:
chr12:g.14659973C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14507039C>G , CM000674.2:g.14507039C>G | GRCh38 |
| NC_000012.11:g.14659973C>G , CM000674.1:g.14659973C>G | GRCh37 |
| NC_000012.10:g.14551240C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240617.10:c.1266G>C MANE Select | ENSP00000240617.5:p.Leu422= | |
| ENST00000240617.9:c.1266G>C | ENSP00000240617.5:p.Leu422= | |
| NM_024829.5:c.1266G>C | NP_079105.4:p.Leu422= | |
| NM_024829.6:c.1266G>C MANE Select | NP_079105.4:p.Leu422= |