Linked Data
MyVariant Identifiers:
chr12:g.52827657C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52433873C>T , CM000674.2:g.52433873C>T | GRCh38 |
| NC_000012.11:g.52827657C>T , CM000674.1:g.52827657C>T | GRCh37 |
| NC_000012.10:g.51113924C>T | NCBI36 |
| NG_008403.1:g.5454G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252245.6:c.432G>A MANE Select | ENSP00000252245.5:p.Arg144= | |
| ENST00000252245.5:c.432G>A | ENSP00000252245.5:p.Arg144= | |
| NM_004693.2:c.432G>A | NP_004684.2:p.Arg144= | |
| NM_004693.3:c.432G>A MANE Select | NP_004684.2:p.Arg144= |