Linked Data
dbSNP Id:
rs2146527849
gnomAD v4:
20-57562883-C-T
MyVariant Identifiers:
chr20:g.56137939C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562883C>T , CM000682.2:g.57562883C>T | GRCh38 |
| NC_000020.10:g.56137939C>T , CM000682.1:g.56137939C>T | GRCh37 |
| NC_000020.9:g.55571345C>T | NCBI36 |
| NG_008205.1:g.6803C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.594C>T MANE Select | ENSP00000319814.4:p.Cys198= | |
| ENST00000319441.5:c.594C>T | ENSP00000319814.4:p.Cys198= | |
| ENST00000467047.1:n.1804C>T | ||
| ENST00000470051.1:n.50C>T | ||
| ENST00000498194.1:n.536C>T | ||
| NM_002591.3:c.594C>T | NP_002582.3:p.Cys198= | |
| XM_011528839.1:c.198C>T | XP_011527141.1:p.Cys66= | |
| XM_024451888.1:c.198C>T | XP_024307656.1:p.Cys66= | |
| NM_002591.4:c.594C>T MANE Select | NP_002582.3:p.Cys198= |