Linked Data
MyVariant Identifiers:
chr20:g.56137801T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562745T>A , CM000682.2:g.57562745T>A | GRCh38 |
| NC_000020.10:g.56137801T>A , CM000682.1:g.56137801T>A | GRCh37 |
| NC_000020.9:g.55571207T>A | NCBI36 |
| NG_008205.1:g.6665T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.456T>A MANE Select | ENSP00000319814.4:p.Pro152= | |
| ENST00000319441.5:c.456T>A | ENSP00000319814.4:p.Pro152= | |
| ENST00000467047.1:n.1666T>A | ||
| ENST00000498194.1:n.398T>A | ||
| NM_002591.3:c.456T>A | NP_002582.3:p.Pro152= | |
| XM_011528839.1:c.60T>A | XP_011527141.1:p.Pro20= | |
| XM_024451888.1:c.60T>A | XP_024307656.1:p.Pro20= | |
| NM_002591.4:c.456T>A MANE Select | NP_002582.3:p.Pro152= |