Canonical Allele Identifier: CA15304306
Gene: UNC5C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11097470

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95546352C>T , CM000666.2:g.95546352C>T GRCh38
NC_000004.11:g.96467503C>T , CM000666.1:g.96467503C>T GRCh37
NC_000004.10:g.96686526C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_003728.3:c.124+2382G>A VV NP_003719.3:p.=
XM_005263321.2:c.124+2382G>A XP_005263378.1:p.=
XM_005263321.3:c.124+2382G>A
ENST00000453304.5:c.124+2382G>A ENSP00000406022.1:p.=
ENST00000504962.1:c.124+2382G>A ENSP00000425117.1:p.=
ENST00000506749.5:c.124+2382G>A ENSP00000426153.1:p.=
ENST00000513796.5:c.124+2382G>A ENSP00000426924.1:p.=