Linked Data
MyVariant Identifiers:
chr12:g.89744552G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.89350775G>T , CM000674.2:g.89350775G>T | GRCh38 |
| NC_000012.11:g.89744552G>T , CM000674.1:g.89744552G>T | GRCh37 |
| NC_000012.10:g.88268683G>T | NCBI36 |
| NG_033915.1:g.7085C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279488.8:c.651C>A MANE Select | ENSP00000279488.6:p.Gly217= | |
| ENST00000279488.7:c.651C>A | ENSP00000279488.6:p.Gly217= | |
| ENST00000308385.6:c.400+865C>A | ENSP00000307835.6:n.400+865C>A | |
| ENST00000547140.1:n.337C>A | ||
| ENST00000547291.1:c.276C>A | ENSP00000449838.1:p.Gly92= | |
| NM_001946.3:c.651C>A | NP_001937.2:p.Gly217= | |
| NM_022652.3:c.400+865C>A | NP_073143.2:n.400+865C>A | |
| NM_001946.4:c.651C>A MANE Select | NP_001937.2:p.Gly217= | |
| NM_022652.4:c.400+865C>A | NP_073143.2:n.400+865C>A |