Linked Data
dbSNP Id:
rs750399240
ExAC:
20:62062653 C / T
gnomAD v2:
20-62062653-C-T
gnomAD v3:
20-63431300-C-T
gnomAD v4:
20-63431300-C-T
MyVariant Identifiers:
chr20:g.62062653C>T (hg19)
chr20:g.62062653_62062655delinsTCA (hg19)
chr20:g.63431300C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63431300C>T , CM000682.2:g.63431300C>T | GRCh38 |
| NC_000020.10:g.62062653C>T , CM000682.1:g.62062653C>T | GRCh37 |
| NC_000020.9:g.61533097C>T | NCBI36 |
| NG_009004.1:g.46341G>A | |
| NG_009004.2:g.46341G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.1148+40G>A | ENSP00000516702.1:n.1148+40G>A | |
| ENST00000359125.7:c.1148+40G>A MANE Select | ENSP00000352035.2:n.1148+40G>A | |
| ENST00000636638.1:n.31+2146G>A | ||
| ENST00000637193.1:c.599+2509G>A | ENSP00000490734.1:n.599+2509G>A | |
| ENST00000344462.8:c.1148+40G>A | ENSP00000339611.4:n.1148+40G>A | |
| ENST00000357249.6:c.806+40G>A | ENSP00000349789.3:n.806+40G>A | |
| ENST00000359125.6:c.1148+40G>A | ENSP00000352035.2:n.1148+40G>A | |
| ENST00000360480.7:c.1118+2509G>A | ENSP00000353668.3:n.1118+2509G>A | |
| ENST00000370221.3:n.1274+40G>A | ||
| ENST00000370224.5:c.1118+2509G>A | ENSP00000359244.2:n.1118+2509G>A | |
| ENST00000625514.2:c.1118+2509G>A | ENSP00000486040.1:n.1118+2509G>A | |
| ENST00000626839.2:c.1148+40G>A | ENSP00000486706.1:n.1148+40G>A | |
| ENST00000627221.2:c.262+2509G>A | ||
| ENST00000629241.2:c.1118+2509G>A | ENSP00000487142.1:n.1118+2509G>A | |
| ENST00000629676.2:c.1118+2509G>A | ENSP00000486194.1:n.1118+2509G>A | |
| NM_004518.4:c.1118+2509G>A | NP_004509.2:n.1118+2509G>A | |
| NM_172106.1:c.1148+40G>A | NP_742104.1:n.1148+40G>A | |
| NM_172107.2:c.1148+40G>A | NP_742105.1:n.1148+40G>A | |
| NM_172108.3:c.1148+40G>A | NP_742106.1:n.1148+40G>A | |
| XM_006723787.1:c.1148+40G>A | XP_006723850.1:n.1148+40G>A | |
| XM_011528807.1:c.1148+40G>A | XP_011527109.1:n.1148+40G>A | |
| XM_011528808.1:c.1148+40G>A | XP_011527110.1:n.1148+40G>A | |
| XM_011528809.1:c.1118+2509G>A | XP_011527111.1:n.1118+2509G>A | |
| XM_011528810.1:c.1148+40G>A | XP_011527112.1:n.1148+40G>A | |
| XM_011528811.1:c.1118+2509G>A | XP_011527113.1:n.1118+2509G>A | |
| XM_011528812.1:c.1148+40G>A | XP_011527114.1:n.1148+40G>A | |
| XM_011528813.1:c.1022+40G>A | XP_011527115.1:n.1022+40G>A | |
| XM_011528814.1:c.629+40G>A | XP_011527116.1:n.629+40G>A | |
| XM_011528815.1:c.1148+40G>A | XP_011527117.1:n.1148+40G>A | |
| NM_004518.5:c.1118+2509G>A | NP_004509.2:n.1118+2509G>A | |
| NM_172106.2:c.1148+40G>A | NP_742104.1:n.1148+40G>A | |
| NM_172107.3:c.1148+40G>A | NP_742105.1:n.1148+40G>A | |
| NM_172108.4:c.1148+40G>A | NP_742106.1:n.1148+40G>A | |
| XM_011528810.2:c.1148+40G>A | XP_011527112.1:n.1148+40G>A | |
| XM_011528811.2:c.1118+2509G>A | XP_011527113.1:n.1118+2509G>A | |
| XM_017027841.2:c.1148+40G>A | XP_016883330.1:n.1148+40G>A | |
| XM_017027842.2:c.1148+40G>A | XP_016883331.1:n.1148+40G>A | |
| XM_017027843.1:c.1079+40G>A | XP_016883332.1:n.1079+40G>A | |
| XM_017027844.2:c.1148+40G>A | XP_016883333.1:n.1148+40G>A | |
| NM_004518.6:c.1118+2509G>A | NP_004509.2:n.1118+2509G>A | |
| NM_172106.3:c.1148+40G>A | NP_742104.1:n.1148+40G>A | |
| NM_172107.4:c.1148+40G>A MANE Select | NP_742105.1:n.1148+40G>A | |
| NM_172108.5:c.1148+40G>A | NP_742106.1:n.1148+40G>A | |
| NM_001382235.1:c.1148+40G>A | NP_001369164.1:n.1148+40G>A |