Canonical Allele Identifier: CA445104698
Gene: AP3B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.77425117G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.78129293G>C , CM000667.2:g.78129293G>C GRCh38
NC_000005.9:g.77425117G>C , CM000667.1:g.77425117G>C GRCh37
NC_000005.8:g.77460873G>C NCBI36
NG_007268.1:g.170412C>G , LRG_170:g.170412C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000517561.2:c.1665C>G ENSP00000511839.1:p.Thr555=
ENST00000517940.2:c.1665C>G ENSP00000511881.1:p.Thr555=
ENST00000519295.6:c.1518C>G ENSP00000430597.1:p.Thr506=
ENST00000519888.6:c.1665C>G ENSP00000511880.1:p.Thr555=
ENST00000695447.1:c.1665C>G ENSP00000511917.1:p.Thr555=
ENST00000695450.1:c.1168-13059C>G ENSP00000511919.1:n.1168-13059C>G
ENST00000695451.1:c.*1431C>G ENSP00000511920.1:n.*1431C>G
ENST00000695453.1:c.1608C>G ENSP00000511921.1:p.Thr536=
ENST00000695454.1:c.1659C>G ENSP00000511922.1:p.Thr553=
ENST00000695455.1:c.1518C>G ENSP00000511923.1:p.Thr506=
ENST00000695488.1:c.1665C>G ENSP00000511959.1:p.Thr555=
ENST00000695505.1:n.1823C>G
ENST00000695507.1:c.1665C>G ENSP00000511970.1:p.Thr555=
ENST00000695510.1:c.1665C>G ENSP00000511973.1:p.Thr555=
ENST00000695511.1:c.1665C>G ENSP00000511974.1:p.Thr555=
ENST00000695512.1:c.1665C>G ENSP00000511975.1:p.Thr555=
ENST00000695513.1:c.1530C>G ENSP00000511976.1:p.Thr510=
ENST00000695514.1:c.1665C>G ENSP00000511977.1:p.Thr555=
ENST00000695515.1:c.1665C>G ENSP00000511978.1:p.Thr555=
ENST00000255194.11:c.1665C>G MANE Select ENSP00000255194.7:p.Thr555=
ENST00000255194.10:c.1665C>G ENSP00000255194.6:p.Thr555=
ENST00000517561.1:n.43C>G
ENST00000519295.5:c.1518C>G ENSP00000430597.1:p.Thr506=
NM_001271769.1:c.1518C>G NP_001258698.1:p.Thr506=
NM_003664.4:c.1665C>G , LRG_170t1:c.1665C>G NP_003655.3:p.Thr555=
XM_005248618.2:c.1665C>G XP_005248675.1:p.Thr555=
XM_005248619.3:c.1665C>G XP_005248676.1:p.Thr555=
XM_005248618.4:c.1665C>G XP_005248675.1:p.Thr555=
XM_005248619.5:c.1665C>G XP_005248676.1:p.Thr555=
XM_017010001.1:c.1518C>G XP_016865490.1:p.Thr506=
NM_001271769.2:c.1518C>G NP_001258698.1:p.Thr506=
NM_003664.5:c.1665C>G MANE Select NP_003655.3:p.Thr555=