Linked Data
MyVariant Identifiers:
chr12:g.65640033A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246253A>T , CM000674.2:g.65246253A>T | GRCh38 |
| NC_000012.11:g.65640033A>T , CM000674.1:g.65640033A>T | GRCh37 |
| NC_000012.10:g.63926300A>T | NCBI36 |
| NG_016210.1:g.81683A>T | |
| NG_016210.2:g.81683A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2664A>T MANE Select | ENSP00000308369.2:p.Ser888= | |
| ENST00000308330.2:c.2664A>T | ENSP00000308369.2:p.Ser888= | |
| ENST00000539442.1:n.646A>T | ||
| ENST00000544506.1:n.384A>T | ||
| ENST00000545026.1:n.482A>T | ||
| NM_001167614.1:c.2661A>T | NP_001161086.1:p.Ser887= | |
| NM_014319.4:c.2664A>T | NP_055134.2:p.Ser888= | |
| NM_014319.5:c.2664A>T MANE Select | NP_055134.2:p.Ser888= | |
| NM_001167614.2:c.2661A>T | NP_001161086.1:p.Ser887= |