Linked Data
MyVariant Identifiers:
chr12:g.65639949G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246169G>A , CM000674.2:g.65246169G>A | GRCh38 |
| NC_000012.11:g.65639949G>A , CM000674.1:g.65639949G>A | GRCh37 |
| NC_000012.10:g.63926216G>A | NCBI36 |
| NG_016210.1:g.81599G>A | |
| NG_016210.2:g.81599G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2580G>A MANE Select | ENSP00000308369.2:p.Leu860= | |
| ENST00000308330.2:c.2580G>A | ENSP00000308369.2:p.Leu860= | |
| ENST00000539442.1:n.562G>A | ||
| ENST00000544506.1:n.300G>A | ||
| ENST00000545026.1:n.398G>A | ||
| NM_001167614.1:c.2577G>A | NP_001161086.1:p.Leu859= | |
| NM_014319.4:c.2580G>A | NP_055134.2:p.Leu860= | |
| NM_014319.5:c.2580G>A MANE Select | NP_055134.2:p.Leu860= | |
| NM_001167614.2:c.2577G>A | NP_001161086.1:p.Leu859= |