Linked Data
MyVariant Identifiers:
chr20:g.56140515G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57565459G>C , CM000682.2:g.57565459G>C | GRCh38 |
| NC_000020.10:g.56140515G>C , CM000682.1:g.56140515G>C | GRCh37 |
| NC_000020.9:g.55573921G>C | NCBI36 |
| NG_008205.1:g.9379G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.1524G>C MANE Select | ENSP00000319814.4:p.Leu508= | |
| ENST00000319441.5:c.1524G>C | ENSP00000319814.4:p.Leu508= | |
| ENST00000467047.1:n.4166G>C | ||
| NM_002591.3:c.1524G>C | NP_002582.3:p.Leu508= | |
| XM_011528839.1:c.1128G>C | XP_011527141.1:p.Leu376= | |
| XM_024451888.1:c.1128G>C | XP_024307656.1:p.Leu376= | |
| NM_002591.4:c.1524G>C MANE Select | NP_002582.3:p.Leu508= |