Linked Data
MyVariant Identifiers:
chr6:g.167754882T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.167341394T>C , CM000668.2:g.167341394T>C | GRCh38 |
| NC_000006.11:g.167754882T>C , CM000668.1:g.167754882T>C | GRCh37 |
| NC_000006.10:g.167674872T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239587.10:c.1494T>C MANE Select | ENSP00000239587.5:p.His498= | |
| ENST00000649884.1:c.1275T>C | ENSP00000497040.1:p.His425= | |
| ENST00000239587.9:c.1494T>C | ENSP00000239587.5:p.His498= | |
| ENST00000515138.1:c.1494T>C | ENSP00000424130.1:p.His498= | |
| NM_031949.4:c.1494T>C | NP_114155.4:p.His498= | |
| XM_006715572.2:c.1275T>C | XP_006715635.1:p.His425= | |
| XM_006715572.4:c.1275T>C | XP_006715635.1:p.His425= | |
| NM_031949.5:c.1494T>C MANE Select | NP_114155.4:p.His498= |