Canonical Allele Identifier: CA5642274
Gene: COX15 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 280009
dbSNP Id: rs200910834

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99727157G>C , CM000672.2:g.99727157G>C GRCh38
NC_000010.10:g.101486914G>C , CM000672.1:g.101486914G>C GRCh37
NC_000010.9:g.101476904G>C NCBI36
NG_008986.1:g.10510C>G , LRG_406:g.10510C>G

Transcript Alleles

HGVS Amino-acid change
NM_004376.5:c.396-3C>G , LRG_406t2:c.396-3C>G NP_004367.2:p.=
NM_078470.4:c.396-3C>G , LRG_406t1:c.396-3C>G NP_510870.1:p.=
XM_005269539.3:c.396-3C>G XP_005269596.1:p.=
XM_006717633.2:c.396-3C>G XP_006717696.1:p.=
XM_006717634.2:c.396-3C>G XP_006717697.1:p.=
XM_011539298.1:c.396-3C>G XP_011537600.1:p.=
NM_001320974.1:c.396-3C>G VV NP_001307903.1:p.=
NM_001320975.1:c.396-3C>G VV NP_001307904.1:p.=
NM_001320976.1:c.-59-86C>G VV NP_001307905.1:p.=
NM_004376.6:c.396-3C>G VV NP_004367.2:p.=
NM_078470.5:c.396-3C>G VV NP_510870.1:p.=
XM_006717634.3:c.396-3C>G XP_006717697.1:p.=
XM_011539298.2:c.396-3C>G XP_011537600.1:p.=
ENST00000016171.5:c.396-3C>G ENSP00000016171.5:p.=
ENST00000370483.9:c.396-3C>G ENSP00000359514.5:p.=
ENST00000493385.5:n.309+4047G>C