Linked Data
MyVariant Identifiers:
chr20:g.10625599G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644951G>A , CM000682.2:g.10644951G>A | GRCh38 |
| NC_000020.10:g.10625599G>A , CM000682.1:g.10625599G>A | GRCh37 |
| NC_000020.9:g.10573599G>A | NCBI36 |
| NG_007496.1:g.34096C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2256C>T MANE Select | ENSP00000254958.4:p.Pro752= | |
| ENST00000617965.2:n.2845C>T | ||
| ENST00000254958.9:c.2256C>T | ENSP00000254958.4:p.Pro752= | |
| ENST00000423891.6:n.2122C>T | ||
| ENST00000488480.2:n.653C>T | ||
| NM_000214.2:c.2256C>T | NP_000205.1:p.Pro752= | |
| NM_000214.3:c.2256C>T MANE Select | NP_000205.1:p.Pro752= |