Linked Data
ClinVar Variation Id:
1515230
dbSNP Id:
rs373926591
ExAC:
19:36224078 C / T
gnomAD v2:
19-36224078-C-T
gnomAD v3:
19-35733177-C-T
gnomAD v4:
19-35733177-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35733177C>T , CM000681.2:g.35733177C>T | GRCh38 |
| NC_000019.9:g.36224078C>T , CM000681.1:g.36224078C>T | GRCh37 |
| NC_000019.8:g.40915918C>T | NCBI36 |
| NG_052906.1:g.20159C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592092.2:n.934C>T | ||
| ENST00000673918.2:c.6562C>T | ENSP00000501283.1:p.Pro2188Ser | |
| ENST00000674114.2:c.4169C>T | ENSP00000501039.2:n.4169C>T | |
| ENST00000684977.1:c.1846C>T | ENSP00000509384.1:p.Pro616Ser | |
| ENST00000689544.1:n.1781C>T | ||
| ENST00000691421.1:c.1849C>T | ENSP00000508674.1:p.Pro617Ser | |
| ENST00000691855.1:c.6170C>T | ||
| ENST00000692961.1:c.6628C>T | ENSP00000509289.1:p.Pro2210Ser | |
| ENST00000693677.1:c.705-420C>T | ENSP00000509779.1:n.705-420C>T | |
| ENST00000420124.4:c.6628C>T MANE Select | ENSP00000398837.2:p.Pro2210Ser | |
| ENST00000673918.1:c.6562C>T | ENSP00000501283.1:p.Pro2188Ser | |
| ENST00000674114.1:c.3950C>T | ||
| ENST00000420124.2:c.6628C>T | ENSP00000398837.1:p.Pro2210Ser | |
| NM_014727.2:c.6628C>T | NP_055542.1:p.Pro2210Ser | |
| XM_011527561.1:c.6562C>T | XP_011525863.1:p.Pro2188Ser | |
| XM_011527562.1:c.6628C>T | XP_011525864.1:p.Pro2210Ser | |
| XM_011527563.1:c.6352C>T | XP_011525865.1:p.Pro2118Ser | |
| XM_011527561.2:c.6064C>T | XP_011525863.2:p.Pro2022Ser | |
| XM_011527562.2:c.6628C>T | XP_011525864.1:p.Pro2210Ser | |
| XM_017027544.1:c.6628C>T | XP_016883033.1:p.Pro2210Ser | |
| XM_017027545.1:c.6064C>T | XP_016883034.1:p.Pro2022Ser | |
| XM_017027546.1:c.3592C>T | XP_016883035.1:p.Pro1198Ser | |
| NM_014727.3:c.6628C>T MANE Select | NP_055542.1:p.Pro2210Ser |