Canonical Allele Identifier: CA7573956
Community Standard Title: NM_004855.5(PIGB):c.847-10A>G

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.55340602A>G , CM000677.2:g.55340602A>G GRCh38
NC_000015.9:g.55632800A>G , CM000677.1:g.55632800A>G GRCh37
NC_000015.8:g.53420092A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004855.5:c.847-10A>G (PIGB) MANE Select NP_004846.4:n.847-10A>G
ENST00000164305.10:c.847-10A>G (PIGB) MANE Select ENSP00000164305.5:n.847-10A>G
NM_004855.4:c.847-10A>G (PIGB) NP_004846.4:n.847-10A>G
ENST00000164305.9:c.847-10A>G (PIGB) ENSP00000164305.5:n.847-10A>G
ENST00000539642.5:c.850-10A>G (PIGB) ENSP00000438963.2:n.850-10A>G
ENST00000563294.1:n.136-150T>C (CCPG1)
ENST00000564663.1:c.243-150T>C (CCPG1)
ENST00000565367.5:c.*83-10A>G (PIGB) ENSP00000455943.1:n.*83-10A>G
ENST00000565402.1:n.230A>G (PIGB)
XM_005254795.3:c.364-10A>G (PIGB) XP_005254852.1:n.364-10A>G
XM_005254795.5:c.364-10A>G (PIGB) XP_005254852.1:n.364-10A>G
XM_011522235.1:c.847-55A>G (PIGB) XP_011520537.1:n.847-55A>G
XM_011522235.3:c.847-55A>G (PIGB) XP_011520537.1:n.847-55A>G
XM_011522236.1:c.742-10A>G (PIGB) XP_011520538.1:n.742-10A>G
XM_011522236.3:c.742-10A>G (PIGB) XP_011520538.1:n.742-10A>G
XM_011522237.1:c.448-10A>G (PIGB) XP_011520539.1:n.448-10A>G
XM_011522237.2:c.448-10A>G (PIGB) XP_011520539.1:n.448-10A>G
XM_017022730.1:c.448-10A>G (PIGB) XP_016878219.1:n.448-10A>G
XM_017022731.1:c.448-10A>G (PIGB) XP_016878220.1:n.448-10A>G
XM_017022732.2:c.364-55A>G (PIGB) XP_016878221.1:n.364-55A>G
XM_024449815.1:c.-76+7730T>C (PIGBOS1) XP_024305583.1:n.-76+7730T>C
XR_001751422.2:n.1159-10A>G (PIGB)
XR_001751423.2:n.1159-55A>G (PIGB)
XR_931950.1:n.1163-10A>G (PIGB)
XR_931950.3:n.1159-10A>G (PIGB)