Linked Data
MyVariant Identifiers:
chr8:g.65528597G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64616040G>C , CM000670.2:g.64616040G>C | GRCh38 |
| NC_000008.10:g.65528597G>C , CM000670.1:g.65528597G>C | GRCh37 |
| NC_000008.9:g.65691151G>C | NCBI36 |
| NG_008338.1:g.187752C>G | |
| NG_008338.2:g.187752C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.501C>G MANE Select | ENSP00000310721.3:p.Pro167= | |
| ENST00000310193.3:c.501C>G | ENSP00000310721.3:p.Pro167= | |
| NM_004820.3:c.501C>G | NP_004811.1:p.Pro167= | |
| NM_001324112.1:c.501C>G | NP_001311041.1:p.Pro167= | |
| NM_004820.4:c.501C>G | NP_004811.1:p.Pro167= | |
| XM_017014002.1:c.567C>G | XP_016869491.1:p.Pro189= | |
| NM_004820.5:c.501C>G MANE Select | NP_004811.1:p.Pro167= | |
| NM_001324112.2:c.501C>G | NP_001311041.1:p.Pro167= |