Canonical Allele Identifier: CA147771856
Gene: RSPO3 HGNC NCBI

Linked Data

dbSNP Id: rs6569474
gnomAD v2: 6-127493611-A-T
gnomAD v3: 6-127172466-A-T
gnomAD v4: 6-127172466-A-T
MyVariant Identifiers: chr6:g.127493611A>T (hg19) chr6:g.127172466A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.127172466A>T , CM000668.2:g.127172466A>T GRCh38
NC_000006.11:g.127493611A>T , CM000668.1:g.127493611A>T GRCh37
NC_000006.10:g.127535304A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356698.9:c.634+17028A>T MANE Select ENSP00000349131.4:n.634+17028A>T
ENST00000650648.1:n.401+4850T>A
ENST00000650684.1:n.473+4850T>A
ENST00000650727.1:n.440+4850T>A
ENST00000650777.1:n.472+4850T>A
ENST00000650823.1:n.448+4850T>A
ENST00000650841.1:n.440+4850T>A
ENST00000650899.1:n.467+4850T>A
ENST00000651038.1:n.471+4850T>A
ENST00000651052.1:n.88+4850T>A
ENST00000651110.1:n.423+4850T>A
ENST00000651273.1:n.489+4850T>A
ENST00000651331.1:n.489+4850T>A
ENST00000651338.1:n.471+4850T>A
ENST00000651421.1:n.746+4850T>A
ENST00000651607.1:n.473+4850T>A
ENST00000651795.1:n.440+4850T>A
ENST00000651850.1:n.489+4850T>A
ENST00000651963.1:n.138+4850T>A
ENST00000652330.1:n.464+4850T>A
ENST00000652419.1:n.91+4850T>A
ENST00000652459.1:n.434+4850T>A
ENST00000652545.1:n.489+4850T>A
ENST00000356698.8:c.634+17028A>T ENSP00000349131.4:n.634+17028A>T
ENST00000368317.3:c.634+17028A>T ENSP00000357300.3:n.634+17028A>T
NM_032784.4:c.634+17028A>T NP_116173.2:n.634+17028A>T
XR_942959.1:n.690+4850T>A
XM_017011378.1:c.634+17028A>T XP_016866867.1:n.634+17028A>T
XM_017011379.1:c.427+17028A>T XP_016866868.1:n.427+17028A>T
XR_002956392.1:n.5657T>A
NM_032784.5:c.634+17028A>T MANE Select NP_116173.2:n.634+17028A>T
Search 100 bp 5'
Search 100 bp 3'