Linked Data
MyVariant Identifiers:
chr12:g.65633924C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65240144C>A , CM000674.2:g.65240144C>A | GRCh38 |
| NC_000012.11:g.65633924C>A , CM000674.1:g.65633924C>A | GRCh37 |
| NC_000012.10:g.63920191C>A | NCBI36 |
| NG_016210.1:g.75574C>A | |
| NG_016210.2:g.75574C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2032C>A MANE Select | ENSP00000308369.2:p.Arg678= | |
| ENST00000308330.2:c.2032C>A | ENSP00000308369.2:p.Arg678= | |
| NM_001167614.1:c.2029C>A | NP_001161086.1:p.Arg677= | |
| NM_014319.4:c.2032C>A | NP_055134.2:p.Arg678= | |
| NM_014319.5:c.2032C>A MANE Select | NP_055134.2:p.Arg678= | |
| NM_001167614.2:c.2029C>A | NP_001161086.1:p.Arg677= |