Canonical Allele Identifier: CA97208807
Gene: COX7B2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11726563

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46821617A>C , CM000666.2:g.46821617A>C GRCh38
NC_000004.10:g.46518391A>C NCBI36
NC_000004.11:g.46823634A>C , CM000666.1:g.46823634A>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000355591.7:c.-50+23343T>G ENSP00000347799.3:p.=
ENST00000396533.5:c.-50+23343T>G ENSP00000379784.1:p.=
ENST00000505102.1:c.-50+23343T>G ENSP00000423519.1:p.=
ENST00000543208.5:c.-53+23343T>G ENSP00000437439.1:p.=
NM_130902.2:c.-50+23343T>G VV NP_570972.2:p.=
XM_011513630.1:c.-50+23343T>G XP_011511932.1:p.=
XM_011513631.1:c.-50+23343T>G XP_011511933.1:p.=
XM_011513632.1:c.-50+23343T>G XP_011511934.1:p.=
XM_011513633.1:c.-50+23343T>G XP_011511935.1:p.=
XM_011513634.1:c.-50+23343T>G XP_011511936.1:p.=
XM_011513635.1:c.-50+23343T>G XP_011511937.1:p.=
XM_011513637.1:c.-50+23343T>G XP_011511939.1:p.=
XM_011513638.1:c.-50+23343T>G XP_011511940.1:p.=