Linked Data
MyVariant Identifiers:
chr12:g.14659988C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14507054C>T , CM000674.2:g.14507054C>T | GRCh38 |
| NC_000012.11:g.14659988C>T , CM000674.1:g.14659988C>T | GRCh37 |
| NC_000012.10:g.14551255C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240617.10:c.1251G>A MANE Select | ENSP00000240617.5:p.Leu417= | |
| ENST00000240617.9:c.1251G>A | ENSP00000240617.5:p.Leu417= | |
| NM_024829.5:c.1251G>A | NP_079105.4:p.Leu417= | |
| NM_024829.6:c.1251G>A MANE Select | NP_079105.4:p.Leu417= |