Linked Data
MyVariant Identifiers:
chr8:g.10470405T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10612895T>A , CM000670.2:g.10612895T>A | GRCh38 |
| NC_000008.10:g.10470405T>A , CM000670.1:g.10470405T>A | GRCh37 |
| NC_000008.9:g.10507815T>A | NCBI36 |
| NG_028035.1:g.47213A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.1203A>T MANE Select | ENSP00000371923.3:p.Pro401= | |
| ENST00000382483.3:c.1203A>T | ENSP00000371923.3:p.Pro401= | |
| NM_178857.5:c.1203A>T | NP_849188.4:p.Pro401= | |
| NM_178857.6:c.1203A>T MANE Select | NP_849188.4:p.Pro401= |