Canonical Allele Identifier: CA1779398775

Gene: POLB

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42369287C= , CM000670.2:g.42369287C=	GRCh38
NC_000008.10:g.42226805C= , CM000670.1:g.42226805C=	GRCh37
NC_000008.9:g.42345962C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002690.3:c.725C= MANE Select	NP_002681.1:p.Pro242=
ENST00000265421.9:c.725C= MANE Select	ENSP00000265421.4:p.Pro242=
NM_002690.2:c.725C=	NP_002681.1:p.Pro242=
ENST00000265421.8:c.725C=	ENSP00000265421.4:p.Pro242=
ENST00000517393.1:c.156-2276C=
ENST00000518579.5:c.298C=
ENST00000518925.5:c.830C=	ENSP00000430784.1:p.Pro277=
ENST00000519771.5:c.*529C=	ENSP00000427799.1:n.*529C=
ENST00000521290.5:c.429C=
ENST00000521492.1:c.-119C=	ENSP00000430831.1:n.-119C=
ENST00000522610.5:c.*250C=	ENSP00000429436.1:n.*250C=
ENST00000524208.5:c.465C=	ENSP00000428578.1:n.465C=
XM_005273535.2:c.830C=	XP_005273592.1:p.Pro277=
XM_005273535.4:c.830C=	XP_005273592.1:p.Pro277=
XM_005273536.2:c.743C=	XP_005273593.1:p.Pro248=
XM_005273536.4:c.743C=	XP_005273593.1:p.Pro248=
XM_005273537.2:c.638C=	XP_005273594.1:p.Pro213=
XM_005273537.4:c.638C=	XP_005273594.1:p.Pro213=
XM_005273538.2:c.383C=	XP_005273595.1:p.Pro128=
XM_005273539.2:c.263C=	XP_005273596.1:p.Pro88=
XM_005273540.3:c.263C=	XP_005273597.1:p.Pro88=
XM_005273540.4:c.263C=	XP_005273597.1:p.Pro88=
XM_006716353.2:c.263C=	XP_006716416.1:p.Pro88=
XM_017013583.1:c.383C=	XP_016869072.1:p.Pro128=
XM_017013584.1:c.263C=	XP_016869073.1:p.Pro88=
XR_001745544.2:n.966C=