Linked Data
MyVariant Identifiers:
chr12:g.65632455T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65238675T>G , CM000674.2:g.65238675T>G | GRCh38 |
| NC_000012.11:g.65632455T>G , CM000674.1:g.65632455T>G | GRCh37 |
| NC_000012.10:g.63918722T>G | NCBI36 |
| NG_016210.1:g.74105T>G | |
| NG_016210.2:g.74105T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.1782T>G MANE Select | ENSP00000308369.2:p.Val594= | |
| ENST00000308330.2:c.1782T>G | ENSP00000308369.2:p.Val594= | |
| NM_001167614.1:c.1779T>G | NP_001161086.1:p.Val593= | |
| NM_014319.4:c.1782T>G | NP_055134.2:p.Val594= | |
| NM_014319.5:c.1782T>G MANE Select | NP_055134.2:p.Val594= | |
| NM_001167614.2:c.1779T>G | NP_001161086.1:p.Val593= |