Linked Data
ClinVar Variation Id:
1077142
ClinVar RCV Id:
RCV001391281
dbSNP Id:
rs2145547497
MyVariant Identifiers:
chr20:g.62045455G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63414102G>A , CM000682.2:g.63414102G>A | GRCh38 |
| NC_000020.10:g.62045455G>A , CM000682.1:g.62045455G>A | GRCh37 |
| NC_000020.9:g.61515899G>A | NCBI36 |
| NG_009004.1:g.63539C>T | |
| NG_009004.2:g.63539C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.1563C>T | ENSP00000516702.1:p.Ser521= | |
| ENST00000359125.7:c.1617C>T MANE Select | ENSP00000352035.2:p.Ser539= | |
| ENST00000637193.1:c.1014C>T | ENSP00000490734.1:p.Ser338= | |
| ENST00000344462.8:c.1524C>T | ENSP00000339611.4:p.Ser508= | |
| ENST00000357249.6:c.1185C>T | ENSP00000349789.3:p.Ser395= | |
| ENST00000359125.6:c.1617C>T | ENSP00000352035.2:p.Ser539= | |
| ENST00000360480.7:c.1533C>T | ENSP00000353668.3:p.Ser511= | |
| ENST00000370224.5:c.1533C>T | ENSP00000359244.2:p.Ser511= | |
| ENST00000625514.2:c.1497C>T | ENSP00000486040.1:p.Ser499= | |
| ENST00000626839.2:c.1563C>T | ENSP00000486706.1:p.Ser521= | |
| ENST00000627221.2:c.674C>T | ||
| ENST00000629241.2:c.1533C>T | ENSP00000487142.1:p.Ser511= | |
| ENST00000629318.1:c.225C>T | ENSP00000487384.1:p.Ser75= | |
| ENST00000629676.2:c.1533C>T | ENSP00000486194.1:p.Ser511= | |
| NM_004518.4:c.1533C>T | NP_004509.2:p.Ser511= | |
| NM_172106.1:c.1563C>T | NP_742104.1:p.Ser521= | |
| NM_172107.2:c.1617C>T | NP_742105.1:p.Ser539= | |
| NM_172108.3:c.1524C>T | NP_742106.1:p.Ser508= | |
| XM_006723787.1:c.1617C>T | XP_006723850.1:p.Ser539= | |
| XM_011528807.1:c.1617C>T | XP_011527109.1:p.Ser539= | |
| XM_011528808.1:c.1614C>T | XP_011527110.1:p.Ser538= | |
| XM_011528809.1:c.1587C>T | XP_011527111.1:p.Ser529= | |
| XM_011528810.1:c.1563C>T | XP_011527112.1:p.Ser521= | |
| XM_011528811.1:c.1533C>T | XP_011527113.1:p.Ser511= | |
| XM_011528812.1:c.1614C>T | XP_011527114.1:p.Ser538= | |
| XM_011528813.1:c.1491C>T | XP_011527115.1:p.Ser497= | |
| XM_011528814.1:c.1098C>T | XP_011527116.1:p.Ser366= | |
| XM_011528815.1:c.1617C>T | XP_011527117.1:p.Ser539= | |
| NM_004518.5:c.1533C>T | NP_004509.2:p.Ser511= | |
| NM_172106.2:c.1563C>T | NP_742104.1:p.Ser521= | |
| NM_172107.3:c.1617C>T | NP_742105.1:p.Ser539= | |
| NM_172108.4:c.1524C>T | NP_742106.1:p.Ser508= | |
| XM_011528810.2:c.1563C>T | XP_011527112.1:p.Ser521= | |
| XM_011528811.2:c.1533C>T | XP_011527113.1:p.Ser511= | |
| XM_017027841.2:c.1560C>T | XP_016883330.1:p.Ser520= | |
| XM_017027842.2:c.1563C>T | XP_016883331.1:p.Ser521= | |
| XM_017027843.1:c.1494C>T | XP_016883332.1:p.Ser498= | |
| XM_017027844.2:c.1560C>T | XP_016883333.1:p.Ser520= | |
| XM_017027845.1:c.525C>T | XP_016883334.1:p.Ser175= | |
| NM_004518.6:c.1533C>T | NP_004509.2:p.Ser511= | |
| NM_172106.3:c.1563C>T | NP_742104.1:p.Ser521= | |
| NM_172107.4:c.1617C>T MANE Select | NP_742105.1:p.Ser539= | |
| NM_172108.5:c.1524C>T | NP_742106.1:p.Ser508= | |
| NM_001382235.1:c.1563C>T | NP_001369164.1:p.Ser521= |