Linked Data
MyVariant Identifiers:
chr6:g.121768152T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121447006T>C , CM000668.2:g.121447006T>C | GRCh38 |
| NC_000006.11:g.121768152T>C , CM000668.1:g.121768152T>C | GRCh37 |
| NC_000006.10:g.121809851T>C | NCBI36 |
| NG_008308.1:g.16408T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.159T>C MANE Select | ENSP00000282561.3:p.Arg53= | |
| ENST00000647564.1:c.159T>C | ENSP00000497565.1:p.Arg53= | |
| ENST00000649003.1:c.159T>C | ENSP00000497283.1:p.Arg53= | |
| ENST00000650427.1:c.159T>C | ENSP00000497367.1:p.Arg53= | |
| ENST00000282561.3:c.159T>C | ENSP00000282561.3:p.Arg53= | |
| NM_000165.4:c.159T>C | NP_000156.1:p.Arg53= | |
| NM_000165.5:c.159T>C MANE Select | NP_000156.1:p.Arg53= |