Canonical Allele Identifier: CA36687836
Gene: CD46 HGNC NCBI
MIR29B2CHG HGNC NCBI

Linked Data

dbSNP Id: rs1028055048

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207785195T>A , CM000663.2:g.207785195T>A GRCh38
NC_000001.10:g.207958540T>A , CM000663.1:g.207958540T>A GRCh37
NC_000001.9:g.206025163T>A NCBI36
NG_009296.1:g.38139T>A , LRG_155:g.38139T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000490278.2:n.2192+89T>A (CD46)
ENST00000496723.2:n.1769+89T>A (CD46)
ENST00000636114.2:n.2711+89T>A (CD46)
ENST00000695777.1:c.1018+89T>A (CD46) ENSP00000512167.1:n.1018+89T>A
ENST00000695778.1:c.973+89T>A (CD46) ENSP00000512168.1:n.973+89T>A
ENST00000695779.1:n.1735+89T>A (CD46)
ENST00000695780.1:c.938-461T>A (CD46) ENSP00000512169.1:n.938-461T>A
ENST00000695781.1:c.*101+89T>A (CD46) ENSP00000512170.1:n.*101+89T>A
ENST00000695782.1:c.973+89T>A (CD46) ENSP00000512171.1:n.973+89T>A
ENST00000695783.1:n.4386+89T>A (CD46)
ENST00000695784.1:c.*144+89T>A (CD46) ENSP00000512172.1:n.*144+89T>A
ENST00000695786.1:n.940+89T>A (CD46)
ENST00000695787.1:n.2376+89T>A (CD46)
ENST00000695788.1:n.597+89T>A (CD46)
ENST00000695789.1:n.2358T>A (CD46)
ENST00000695790.1:n.2347T>A (CD46)
ENST00000367042.6:c.1018+89T>A (CD46) MANE Select ENSP00000356009.1:n.1018+89T>A
ENST00000636114.1:n.772+89T>A (CD46)
ENST00000322875.8:c.1063+89T>A (CD46) ENSP00000313875.4:n.1063+89T>A
ENST00000322918.9:c.973+89T>A (CD46) ENSP00000314664.5:n.973+89T>A
ENST00000354848.5:c.1018+89T>A (CD46) ENSP00000346912.1:n.1018+89T>A
ENST00000357714.5:c.973+89T>A (CD46) ENSP00000350346.1:n.973+89T>A
ENST00000358170.6:c.1063+89T>A (CD46) ENSP00000350893.2:n.1063+89T>A
ENST00000360212.6:c.931+89T>A (CD46) ENSP00000353342.2:n.931+89T>A
ENST00000367041.5:c.973+89T>A (CD46) ENSP00000356008.1:n.973+89T>A
ENST00000367042.5:c.1018+89T>A (CD46) ENSP00000356009.1:n.1018+89T>A
ENST00000367047.5:c.874+89T>A (CD46) ENSP00000356014.1:n.874+89T>A
ENST00000462968.2:c.99+89T>A (CD46)
ENST00000469535.5:n.5767+89T>A (CD46)
ENST00000471987.1:n.128+89T>A (CD46)
ENST00000480003.5:c.976+89T>A (CD46) ENSP00000418471.1:n.976+89T>A
ENST00000488596.5:n.397+89T>A (CD46)
NM_002389.4:c.1063+89T>A , LRG_155t1:c.1063+89T>A (CD46) NP_002380.3:n.1063+89T>A
NM_153826.3:c.1018+89T>A (CD46) NP_722548.1:n.1018+89T>A
NM_172350.2:c.973+89T>A (CD46) NP_758860.1:n.973+89T>A
NM_172351.2:c.1018+89T>A (CD46) NP_758861.1:n.1018+89T>A
NM_172352.2:c.973+89T>A (CD46) NP_758862.1:n.973+89T>A
NM_172353.2:c.973+89T>A (CD46) NP_758863.1:n.973+89T>A
NM_172359.2:c.1063+89T>A (CD46) NP_758869.1:n.1063+89T>A
NM_172361.2:c.931+89T>A (CD46) NP_758871.1:n.931+89T>A
XM_011509563.1:c.1021+89T>A (CD46) XP_011507865.1:n.1021+89T>A
XM_011509564.1:c.976+89T>A (CD46) XP_011507866.1:n.976+89T>A
XR_922496.1:n.7666+20810A>T (MIR29B2CHG)
XR_922497.1:n.6306-22207A>T (MIR29B2CHG)
NM_172355.2:c.976+89T>A (CD46) NP_758865.1:n.976+89T>A
NM_172356.2:c.976+89T>A (CD46) NP_758866.1:n.976+89T>A
NM_172357.2:c.931+89T>A (CD46) NP_758867.1:n.931+89T>A
NM_172358.2:c.1018+89T>A (CD46) NP_758868.1:n.1018+89T>A
XM_011509563.2:c.1021+89T>A (CD46) XP_011507865.1:n.1021+89T>A
XM_017001308.2:c.1021+89T>A (CD46) XP_016856797.1:n.1021+89T>A
XR_001737177.2:n.2169+89T>A (CD46)
XR_002956621.1:n.2707+89T>A (CD46)
XR_002956622.1:n.2707+89T>A (CD46)
NM_153826.4:c.1018+89T>A (CD46) NP_722548.1:n.1018+89T>A
NM_172350.3:c.973+89T>A (CD46) NP_758860.1:n.973+89T>A
NM_172351.3:c.1018+89T>A (CD46) MANE Select NP_758861.1:n.1018+89T>A
NM_172352.3:c.973+89T>A (CD46) NP_758862.1:n.973+89T>A
NM_172353.3:c.973+89T>A (CD46) NP_758863.1:n.973+89T>A
NM_172355.3:c.976+89T>A (CD46) NP_758865.1:n.976+89T>A
NM_172356.3:c.976+89T>A (CD46) NP_758866.1:n.976+89T>A
NM_172357.3:c.931+89T>A (CD46) NP_758867.1:n.931+89T>A
NM_172358.3:c.1018+89T>A (CD46) NP_758868.1:n.1018+89T>A
NM_172359.3:c.1063+89T>A (CD46) NP_758869.1:n.1063+89T>A
NM_172361.3:c.931+89T>A (CD46) NP_758871.1:n.931+89T>A