Canonical Allele Identifier: CA15555037

Gene: POLB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42355738G>A , CM000670.2:g.42355738G>A	GRCh38
NC_000008.10:g.42213256G>A , CM000670.1:g.42213256G>A	GRCh37
NC_000008.9:g.42332413G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265421.9:c.422+171G>A MANE Select	ENSP00000265421.4:n.422+171G>A
ENST00000265421.8:c.422+171G>A	ENSP00000265421.4:n.422+171G>A
ENST00000518925.5:c.527+171G>A	ENSP00000430784.1:n.527+171G>A
ENST00000519524.1:n.109+171G>A
ENST00000519771.5:c.*226+171G>A	ENSP00000427799.1:n.*226+171G>A
ENST00000520008.5:c.-41+171G>A	ENSP00000430610.1:n.-41+171G>A
ENST00000521290.5:c.213+171G>A
ENST00000522610.5:c.422+171G>A	ENSP00000429436.1:n.422+171G>A
ENST00000524208.5:c.162+171G>A	ENSP00000428578.1:n.162+171G>A
ENST00000532157.5:c.80+171G>A	ENSP00000432084.1:n.80+171G>A
NM_002690.2:c.422+171G>A	NP_002681.1:n.422+171G>A
XM_005273535.2:c.527+171G>A	XP_005273592.1:n.527+171G>A
XM_005273536.2:c.527+171G>A	XP_005273593.1:n.527+171G>A
XM_005273537.2:c.422+171G>A	XP_005273594.1:n.422+171G>A
XM_005273538.2:c.80+171G>A	XP_005273595.1:n.80+171G>A
XM_005273539.2:c.-41+171G>A	XP_005273596.1:n.-41+171G>A
XM_005273540.3:c.-41+171G>A	XP_005273597.1:n.-41+171G>A
XM_006716353.2:c.-41+171G>A	XP_006716416.1:n.-41+171G>A
XR_428311.1:n.661+171G>A
XM_005273535.4:c.527+171G>A	XP_005273592.1:n.527+171G>A
XM_005273536.4:c.527+171G>A	XP_005273593.1:n.527+171G>A
XM_005273537.4:c.422+171G>A	XP_005273594.1:n.422+171G>A
XM_005273540.4:c.-41+171G>A	XP_005273597.1:n.-41+171G>A
XM_017013583.1:c.80+171G>A	XP_016869072.1:n.80+171G>A
XM_017013584.1:c.-41+171G>A	XP_016869073.1:n.-41+171G>A
XR_001745544.2:n.556+171G>A
XR_428311.3:n.661+171G>A
NM_002690.3:c.422+171G>A MANE Select	NP_002681.1:n.422+171G>A