Canonical Allele Identifier: CA15865455
Gene: C16orf62 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs226849

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19583771G>A , CM000678.2:g.19583771G>A GRCh38
NC_000016.9:g.19595093G>A , CM000678.1:g.19595093G>A GRCh37
NC_000016.8:g.19502594G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001300743.1:c.906+2118G>A VV NP_001287672.1:p.=
NM_020314.5:c.906+2118G>A VV NP_064710.4:p.=
XM_005255435.2:c.906+2118G>A XP_005255492.1:p.=
XM_006721065.2:c.906+2118G>A XP_006721128.1:p.=
XM_011545895.1:c.906+2118G>A XP_011544197.1:p.=
XM_011545896.1:c.-321+2118G>A XP_011544198.1:p.=
NM_001300743.2:c.639+2118G>A VV NP_001287672.2:p.=
NM_001365293.1:c.639+2118G>A VV NP_001352222.1:p.=
NM_001365294.1:c.639+2118G>A VV NP_001352223.1:p.=
NM_001365295.1:c.-321+2118G>A VV NP_001352224.1:p.=
NM_020314.6:c.639+2118G>A VV NP_064710.5:p.=
NR_158160.1:n.666+2118G>A
NR_158161.1:n.666+2118G>A
ENST00000251143.9:c.906+2118G>A ENSP00000251143.6:p.=
ENST00000417362.6:c.639+2118G>A ENSP00000395973.3:p.=
ENST00000438132.7:c.906+2118G>A ENSP00000400815.3:p.=
ENST00000448695.5:c.274+2117G>A ENSP00000398009.2:p.=
ENST00000513947.8:c.639+2118G>A ENSP00000458116.3:p.=
ENST00000539322.5:c.*139+2118G>A ENSP00000438852.1:p.=
ENST00000542263.5:c.906+2118G>A ENSP00000442468.1:p.=
ENST00000543152.5:c.-30+2118G>A ENSP00000457973.1:p.=