Linked Data
MyVariant Identifiers:
chr6:g.49426973T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49459260T>G , CM000668.2:g.49459260T>G | GRCh38 |
| NC_000006.11:g.49426973T>G , CM000668.1:g.49426973T>G | GRCh37 |
| NC_000006.10:g.49534932T>G | NCBI36 |
| NG_007100.1:g.8880A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.207A>C MANE Select | ENSP00000274813.3:p.Ile69= | |
| ENST00000274813.3:c.207A>C | ENSP00000274813.3:p.Ile69= | |
| NM_000255.3:c.207A>C | NP_000246.2:p.Ile69= | |
| XM_005249143.2:c.207A>C | XP_005249200.1:p.Ile69= | |
| XM_005249143.3:c.207A>C | XP_005249200.1:p.Ile69= | |
| NM_000255.4:c.207A>C MANE Select | NP_000246.2:p.Ile69= |