Linked Data
MyVariant Identifiers:
chr8:g.10470353T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10612843T>G , CM000670.2:g.10612843T>G | GRCh38 |
| NC_000008.10:g.10470353T>G , CM000670.1:g.10470353T>G | GRCh37 |
| NC_000008.9:g.10507763T>G | NCBI36 |
| NG_028035.1:g.47265A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.1255A>C MANE Select | ENSP00000371923.3:p.Arg419= | |
| ENST00000382483.3:c.1255A>C | ENSP00000371923.3:p.Arg419= | |
| NM_178857.5:c.1255A>C | NP_849188.4:p.Arg419= | |
| NM_178857.6:c.1255A>C MANE Select | NP_849188.4:p.Arg419= |