Linked Data
MyVariant Identifiers:
chr5:g.45645323A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.45645221A>C , CM000667.2:g.45645221A>C | GRCh38 |
| NC_000005.9:g.45645323A>C , CM000667.1:g.45645323A>C | GRCh37 |
| NC_000005.8:g.45681080A>C | NCBI36 |
| NG_042183.1:g.55898T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303230.6:c.813T>G MANE Select | ENSP00000307342.4:p.Leu271= | |
| ENST00000637256.1:n.41T>G | ||
| ENST00000673735.1:c.813T>G | ENSP00000501107.1:p.Leu271= | |
| ENST00000303230.5:c.813T>G | ENSP00000307342.4:p.Leu271= | |
| ENST00000634658.1:c.813T>G | ENSP00000489134.1:p.Leu271= | |
| NM_021072.3:c.813T>G | NP_066550.2:p.Leu271= | |
| NM_021072.4:c.813T>G MANE Select | NP_066550.2:p.Leu271= |