Canonical Allele Identifier: CA127514423
Gene: CCDC192 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12523164

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127726279T>C , CM000667.2:g.127726279T>C GRCh38
NC_000005.9:g.127061971T>C , CM000667.1:g.127061971T>C GRCh37
NC_000005.8:g.127089870T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_159059.3:n.203+18519T>C
XR_246581.3:n.137+18519T>C
XR_948749.1:n.128+18519T>C
XR_948750.1:n.296+18519T>C
XR_948751.1:n.300+16201T>C
XR_948753.1:n.206+18519T>C
XR_948754.1:n.205+18519T>C
XR_948755.1:n.204+18519T>C
XR_948756.1:n.204+18519T>C
XR_948757.1:n.204+18519T>C
XR_948758.1:n.204+18519T>C
XR_948759.1:n.204+18519T>C
XR_948760.1:n.223+18519T>C
XR_948761.1:n.223+18519T>C
XR_948762.1:n.204+18519T>C
XR_948763.1:n.206+18519T>C
XR_948764.1:n.205+18519T>C
XR_948765.1:n.204+18519T>C
XR_948766.1:n.204+18519T>C
NM_001317938.1:n.171+18519T>C VV NP_001304867.1:p.=
XM_017009806.2:c.51+18519T>C XP_016865295.1:p.=
XM_017009807.1:c.51+18519T>C XP_016865296.1:p.=
XM_017009809.2:c.171+18519T>C XP_016865298.1:p.=
XM_017009810.2:c.171+18519T>C XP_016865299.1:p.=
XM_017009811.2:c.171+18519T>C XP_016865300.1:p.=
XM_017009812.2:c.171+18519T>C XP_016865301.1:p.=
XM_017009813.2:c.171+18519T>C XP_016865302.1:p.=
XM_024446203.1:c.51+18519T>C XP_024301971.1:p.=
XR_002956177.1:n.137+18519T>C
XR_948757.3:n.204+18519T>C