Linked Data
MyVariant Identifiers:
chr6:g.121768056A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121446910A>C , CM000668.2:g.121446910A>C | GRCh38 |
| NC_000006.11:g.121768056A>C , CM000668.1:g.121768056A>C | GRCh37 |
| NC_000006.10:g.121809755A>C | NCBI36 |
| NG_008308.1:g.16312A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.63A>C MANE Select | ENSP00000282561.3:p.Gly21= | |
| ENST00000647564.1:c.63A>C | ENSP00000497565.1:p.Gly21= | |
| ENST00000649003.1:c.63A>C | ENSP00000497283.1:p.Gly21= | |
| ENST00000650427.1:c.63A>C | ENSP00000497367.1:p.Gly21= | |
| ENST00000282561.3:c.63A>C | ENSP00000282561.3:p.Gly21= | |
| NM_000165.4:c.63A>C | NP_000156.1:p.Gly21= | |
| NM_000165.5:c.63A>C MANE Select | NP_000156.1:p.Gly21= |