Linked Data
dbSNP Id:
rs1568997480
gnomAD v2:
20-62127437-G-A
MyVariant Identifiers:
chr20:g.62127437G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63496084G>A , CM000682.2:g.63496084G>A | GRCh38 |
| NC_000020.10:g.62127437G>A , CM000682.1:g.62127437G>A | GRCh37 |
| NC_000020.9:g.61597881G>A | NCBI36 |
| NG_034083.1:g.8232C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706948.1:c.145-49C>T | ENSP00000516668.1:n.145-49C>T | |
| ENST00000706949.1:c.145-49C>T | ENSP00000516669.1:n.145-49C>T | |
| ENST00000217182.6:c.145-49C>T MANE Select | ENSP00000217182.3:n.145-49C>T | |
| ENST00000298049.12:c.145-49C>T | ENSP00000298049.8:n.145-49C>T | |
| ENST00000642899.1:c.145-49C>T | ENSP00000493767.1:n.145-49C>T | |
| ENST00000645357.1:c.145-49C>T | ENSP00000494971.1:n.145-49C>T | |
| ENST00000645586.1:n.2665C>T | ||
| ENST00000646335.1:c.145-49C>T | ENSP00000494752.1:n.145-49C>T | |
| ENST00000675519.1:c.148C>T | ENSP00000501859.1:p.Leu50Phe | |
| ENST00000217182.4:c.145-49C>T | ENSP00000217182.3:n.145-49C>T | |
| ENST00000298049.11:c.145-49C>T | ENSP00000298049.7:n.145-49C>T | |
| NM_001958.3:c.145-49C>T | NP_001949.1:n.145-49C>T | |
| NM_001958.4:c.145-49C>T | NP_001949.1:n.145-49C>T | |
| NM_001958.5:c.145-49C>T MANE Select | NP_001949.1:n.145-49C>T |