Linked Data
ClinVar Variation Id:
281479
ClinVar RCV Id:
RCV000280179
RCV000335257
RCV000338681
RCV000398390
RCV000656969
RCV000818112
RCV001266921
RCV001731554
dbSNP Id:
rs536304635
ExAC:
19:39017654 C / T
gnomAD v2:
19-39017654-C-T
gnomAD v3:
19-38527014-C-T
gnomAD v4:
19-38527014-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38527014C>T , CM000681.2:g.38527014C>T | GRCh38 |
| NC_000019.9:g.39017654C>T , CM000681.1:g.39017654C>T | GRCh37 |
| NC_000019.8:g.43709494C>T | NCBI36 |
| NG_008866.1:g.98315C>T , LRG_766:g.98315C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.10587C>T | ENSP00000471601.2:n.10587C>T | |
| ENST00000359596.8:c.10648C>T MANE Select | ENSP00000352608.2:p.Arg3550Trp | |
| ENST00000355481.8:c.10633C>T | ENSP00000347667.3:p.Arg3545Trp | |
| ENST00000359596.7:c.10648C>T | ENSP00000352608.2:p.Arg3550Trp | |
| ENST00000360985.7:c.10630C>T | ENSP00000354254.4:p.Arg3544Trp | |
| ENST00000594335.5:c.4035C>T | ||
| ENST00000599547.5:c.1455C>T | ||
| NM_000540.2:c.10648C>T , LRG_766t1:c.10648C>T | NP_000531.2:p.Arg3550Trp | |
| NM_001042723.1:c.10633C>T | NP_001036188.1:p.Arg3545Trp | |
| XM_006723317.1:c.10648C>T | XP_006723380.1:p.Arg3550Trp | |
| XM_006723319.1:c.10633C>T | XP_006723382.1:p.Arg3545Trp | |
| XM_011527204.1:c.10645C>T | XP_011525506.1:p.Arg3549Trp | |
| XM_011527205.1:c.10648C>T | XP_011525507.1:p.Arg3550Trp | |
| XM_006723317.2:c.10648C>T | XP_006723380.1:p.Arg3550Trp | |
| XM_006723319.2:c.10633C>T | XP_006723382.1:p.Arg3545Trp | |
| XM_011527205.2:c.10648C>T | XP_011525507.1:p.Arg3550Trp | |
| XR_001753936.1:n.510G>A | ||
| NM_000540.3:c.10648C>T MANE Select | NP_000531.2:p.Arg3550Trp | |
| NM_001042723.2:c.10633C>T | NP_001036188.1:p.Arg3545Trp |