Canonical Allele Identifier: CA899601654
Gene: PIK3CB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138759702G>C , CM000665.2:g.138759702G>C GRCh38
NC_000003.11:g.138478544G>C , CM000665.1:g.138478544G>C GRCh37
NC_000003.10:g.139961234G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674063.1:c.-16-343C>G MANE Select ENSP00000501150.1:n.-16-343C>G
ENST00000461451.1:c.-16-343C>G ENSP00000420399.1:n.-16-343C>G
ENST00000462898.5:c.-16-343C>G ENSP00000420108.1:n.-16-343C>G
ENST00000465581.1:c.-16-343C>G ENSP00000417329.1:n.-16-343C>G
ENST00000477593.5:c.-16-343C>G ENSP00000418143.1:n.-16-343C>G
ENST00000483968.5:c.-16-343C>G ENSP00000419857.1:n.-16-343C>G
XM_005247530.2:c.-16-343C>G XP_005247587.1:n.-16-343C>G
XM_006713659.2:c.-16-343C>G XP_006713722.1:n.-16-343C>G
XM_011512895.1:c.-16-343C>G XP_011511197.1:n.-16-343C>G
XM_006713659.3:c.-16-343C>G XP_006713722.1:n.-16-343C>G
XM_011512895.2:c.-16-343C>G XP_011511197.1:n.-16-343C>G
XM_017006619.1:c.-16-343C>G XP_016862108.1:n.-16-343C>G
NM_006219.3:c.-16-343C>G MANE Select NP_006210.1:n.-16-343C>G
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