Linked Data
ClinVar Variation Id:
2153834
ClinVar RCV Id:
RCV003077816
dbSNP Id:
rs576877652
ExAC:
21:47558476 C / T
gnomAD v2:
21-47558476-C-T
gnomAD v3:
21-46138562-C-T
gnomAD v4:
21-46138562-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46138562C>T , CM000683.2:g.46138562C>T | GRCh38 |
| NC_000021.8:g.47558476C>T , CM000683.1:g.47558476C>T | GRCh37 |
| NC_000021.7:g.46382904C>T | NCBI36 |
| NG_016191.1:g.22006G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460011.6:c.-76G>A | ENSP00000507070.1:n.-76G>A | |
| ENST00000494498.2:c.123G>A | ENSP00000507847.1:p.Pro41= | |
| ENST00000397746.8:c.1389G>A MANE Select | ENSP00000380854.3:p.Pro463= | |
| ENST00000291670.9:c.1389G>A | ENSP00000291670.5:p.Pro463= | |
| ENST00000397743.1:c.1345G>A | ENSP00000380851.1:p.Gly449Ser | |
| ENST00000397746.7:c.1389G>A | ENSP00000380854.3:p.Pro463= | |
| ENST00000397748.5:c.1389G>A | ENSP00000380856.1:p.Pro463= | |
| ENST00000446405.5:c.11G>A | ||
| ENST00000460011.5:n.718G>A | ||
| ENST00000488577.1:n.415G>A | ||
| ENST00000494498.1:n.690G>A | ||
| ENST00000498355.6:n.1458G>A | ||
| NM_006657.2:c.1389G>A | NP_006648.1:p.Pro463= | |
| NM_206965.1:c.1389G>A | NP_996848.1:p.Pro463= | |
| XM_006723961.2:c.1638G>A | XP_006724024.2:p.Pro546= | |
| XM_006723962.2:c.1638G>A | XP_006724025.2:p.Pro546= | |
| XM_011529434.1:c.1638G>A | XP_011527736.1:p.Pro546= | |
| XM_011529435.1:c.1509G>A | XP_011527737.1:p.Pro503= | |
| XM_011529436.1:c.1638G>A | XP_011527738.1:p.Pro546= | |
| XM_011529437.1:c.1638G>A | XP_011527739.1:p.Pro546= | |
| XM_011529438.1:c.1509G>A | XP_011527740.1:p.Pro503= | |
| XM_011529439.1:c.1125G>A | XP_011527741.1:p.Pro375= | |
| XR_937433.1:n.1821G>A | ||
| NM_001320412.1:c.1389G>A | NP_001307341.1:p.Pro463= | |
| XM_006723961.4:c.1638G>A | XP_006724024.2:p.Pro546= | |
| XM_006723962.4:c.1638G>A | XP_006724025.2:p.Pro546= | |
| XM_011529434.3:c.1638G>A | XP_011527736.1:p.Pro546= | |
| XM_011529435.3:c.1509G>A | XP_011527737.1:p.Pro503= | |
| XM_011529436.3:c.1638G>A | XP_011527738.1:p.Pro546= | |
| XM_011529437.3:c.1638G>A | XP_011527739.1:p.Pro546= | |
| XM_011529439.2:c.1125G>A | XP_011527741.1:p.Pro375= | |
| XR_937433.3:n.1855G>A | ||
| NM_206965.2:c.1389G>A MANE Select | NP_996848.1:p.Pro463= | |
| NM_001320412.2:c.1389G>A | NP_001307341.1:p.Pro463= | |
| NM_006657.3:c.1389G>A | NP_006648.1:p.Pro463= |