Linked Data
dbSNP Id:
rs767450776
ExAC:
19:36223820 C / T
gnomAD v3:
19-35732919-C-T
gnomAD v4:
19-35732919-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35732919C>T , CM000681.2:g.35732919C>T | GRCh38 |
| NC_000019.9:g.36223820C>T , CM000681.1:g.36223820C>T | GRCh37 |
| NC_000019.8:g.40915660C>T | NCBI36 |
| NG_052906.1:g.19901C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592092.2:n.676C>T | ||
| ENST00000673918.2:c.6304C>T | ENSP00000501283.1:p.Pro2102Ser | |
| ENST00000674114.2:c.3911C>T | ENSP00000501039.2:n.3911C>T | |
| ENST00000684977.1:c.1588C>T | ENSP00000509384.1:p.Pro530Ser | |
| ENST00000689544.1:n.1523C>T | ||
| ENST00000691421.1:c.1591C>T | ENSP00000508674.1:p.Pro531Ser | |
| ENST00000691855.1:c.5912C>T | ||
| ENST00000692961.1:c.6370C>T | ENSP00000509289.1:p.Pro2124Ser | |
| ENST00000693677.1:c.704+590C>T | ENSP00000509779.1:n.704+590C>T | |
| ENST00000420124.4:c.6370C>T MANE Select | ENSP00000398837.2:p.Pro2124Ser | |
| ENST00000673918.1:c.6304C>T | ENSP00000501283.1:p.Pro2102Ser | |
| ENST00000674114.1:c.3692C>T | ||
| ENST00000420124.2:c.6370C>T | ENSP00000398837.1:p.Pro2124Ser | |
| NM_014727.2:c.6370C>T | NP_055542.1:p.Pro2124Ser | |
| XM_011527561.1:c.6304C>T | XP_011525863.1:p.Pro2102Ser | |
| XM_011527562.1:c.6370C>T | XP_011525864.1:p.Pro2124Ser | |
| XM_011527563.1:c.6094C>T | XP_011525865.1:p.Pro2032Ser | |
| XM_011527561.2:c.5806C>T | XP_011525863.2:p.Pro1936Ser | |
| XM_011527562.2:c.6370C>T | XP_011525864.1:p.Pro2124Ser | |
| XM_017027544.1:c.6370C>T | XP_016883033.1:p.Pro2124Ser | |
| XM_017027545.1:c.5806C>T | XP_016883034.1:p.Pro1936Ser | |
| XM_017027546.1:c.3334C>T | XP_016883035.1:p.Pro1112Ser | |
| NM_014727.3:c.6370C>T MANE Select | NP_055542.1:p.Pro2124Ser |