Linked Data
MyVariant Identifiers:
chr8:g.87645097T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86632869T>C , CM000670.2:g.86632869T>C | GRCh38 |
| NC_000008.10:g.87645097T>C , CM000670.1:g.87645097T>C | GRCh37 |
| NC_000008.9:g.87714213T>C | NCBI36 |
| NG_016980.1:g.115807A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1203A>G MANE Select | ENSP00000316605.5:p.Ala401= | |
| ENST00000681546.1:n.1023A>G | ||
| ENST00000681746.1:c.1203A>G | ENSP00000505959.1:p.Ala401= | |
| ENST00000320005.5:c.1203A>G | ENSP00000316605.5:p.Ala401= | |
| NM_019098.4:c.1203A>G | NP_061971.3:p.Ala401= | |
| XM_011517138.1:c.789A>G | XP_011515440.1:p.Ala263= | |
| XM_011517138.2:c.789A>G | XP_011515440.1:p.Ala263= | |
| NM_019098.5:c.1203A>G MANE Select | NP_061971.3:p.Ala401= |