Linked Data
MyVariant Identifiers:
chr12:g.65640102C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246322C>A , CM000674.2:g.65246322C>A | GRCh38 |
| NC_000012.11:g.65640102C>A , CM000674.1:g.65640102C>A | GRCh37 |
| NC_000012.10:g.63926369C>A | NCBI36 |
| NG_016210.1:g.81752C>A | |
| NG_016210.2:g.81752C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2733C>A MANE Select | ENSP00000308369.2:p.Ser911= | |
| ENST00000308330.2:c.2733C>A | ENSP00000308369.2:p.Ser911= | |
| ENST00000539442.1:n.715C>A | ||
| ENST00000545026.1:n.551C>A | ||
| NM_001167614.1:c.2730C>A | NP_001161086.1:p.Ser910= | |
| NM_014319.4:c.2733C>A | NP_055134.2:p.Ser911= | |
| NM_014319.5:c.2733C>A MANE Select | NP_055134.2:p.Ser911= | |
| NM_001167614.2:c.2730C>A | NP_001161086.1:p.Ser910= |