Canonical Allele Identifier: CA851896366
Gene: POLB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42338923C>G , CM000670.2:g.42338923C>G GRCh38
NC_000008.10:g.42196441C>G , CM000670.1:g.42196441C>G GRCh37
NC_000008.9:g.42315598C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265421.9:c.62-89C>G MANE Select ENSP00000265421.4:n.62-89C>G
ENST00000265421.8:c.62-89C>G ENSP00000265421.4:n.62-89C>G
ENST00000518925.5:c.62-89C>G ENSP00000430784.1:n.62-89C>G
ENST00000519094.5:n.193-89C>G
ENST00000519771.5:c.62-89C>G ENSP00000427799.1:n.62-89C>G
ENST00000520008.5:c.-344+238C>G ENSP00000430610.1:n.-344+238C>G
ENST00000522297.1:n.193-89C>G
ENST00000522610.5:c.62-89C>G ENSP00000429436.1:n.62-89C>G
ENST00000530566.1:n.135+295C>G
ENST00000532157.5:c.-329+238C>G ENSP00000432084.1:n.-329+238C>G
NM_002690.2:c.62-89C>G NP_002681.1:n.62-89C>G
XM_005273535.2:c.62-89C>G XP_005273592.1:n.62-89C>G
XM_005273536.2:c.62-89C>G XP_005273593.1:n.62-89C>G
XM_005273537.2:c.62-89C>G XP_005273594.1:n.62-89C>G
XM_005273538.2:c.-329+238C>G XP_005273595.1:n.-329+238C>G
XM_005273539.2:c.-344+238C>G XP_005273596.1:n.-344+238C>G
XM_005273540.3:c.-160+238C>G XP_005273597.1:n.-160+238C>G
XM_006716353.2:c.-217-89C>G XP_006716416.1:n.-217-89C>G
XR_428311.1:n.196-89C>G
XM_005273535.4:c.62-89C>G XP_005273592.1:n.62-89C>G
XM_005273536.4:c.62-89C>G XP_005273593.1:n.62-89C>G
XM_005273537.4:c.62-89C>G XP_005273594.1:n.62-89C>G
XM_005273540.4:c.-160+238C>G XP_005273597.1:n.-160+238C>G
XM_017013583.1:c.-195+238C>G XP_016869072.1:n.-195+238C>G
XM_017013584.1:c.-210+238C>G XP_016869073.1:n.-210+238C>G
XR_001745544.2:n.196-89C>G
XR_428311.3:n.196-89C>G
NM_002690.3:c.62-89C>G MANE Select NP_002681.1:n.62-89C>G
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