Linked Data
MyVariant Identifiers:
chr12:g.53207831T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814047T>C , CM000674.2:g.52814047T>C | GRCh38 |
| NC_000012.11:g.53207831T>C , CM000674.1:g.53207831T>C | GRCh37 |
| NC_000012.10:g.51494098T>C | NCBI36 |
| NG_007380.1:g.5505A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.2:c.12A>G MANE Select | ENSP00000448220.1:p.Arg4= | |
| ENST00000548097.5:c.12A>G | ENSP00000449755.1:p.Arg4= | |
| ENST00000551956.1:c.12A>G | ENSP00000448220.1:p.Arg4= | |
| ENST00000552668.1:c.12A>G | ENSP00000447320.1:p.Arg4= | |
| NM_002272.3:c.12A>G | NP_002263.3:p.Arg4= | |
| NM_002272.4:c.12A>G MANE Select | NP_002263.3:p.Arg4= |