Linked Data
MyVariant Identifiers:
chr12:g.53207804C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814020C>G , CM000674.2:g.52814020C>G | GRCh38 |
| NC_000012.11:g.53207804C>G , CM000674.1:g.53207804C>G | GRCh37 |
| NC_000012.10:g.51494071C>G | NCBI36 |
| NG_007380.1:g.5532G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.2:c.39G>C MANE Select | ENSP00000448220.1:p.Arg13= | |
| ENST00000548097.5:c.39G>C | ENSP00000449755.1:p.Arg13= | |
| ENST00000551956.1:c.39G>C | ENSP00000448220.1:p.Arg13= | |
| ENST00000552668.1:c.39G>C | ENSP00000447320.1:p.Arg13= | |
| NM_002272.3:c.39G>C | NP_002263.3:p.Arg13= | |
| NM_002272.4:c.39G>C MANE Select | NP_002263.3:p.Arg13= |