Canonical Allele Identifier: CA2830536900

Gene: POLR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56986532T>C , CM000666.2:g.56986532T>C	GRCh38
NC_000004.11:g.57852698T>C , CM000666.1:g.57852698T>C	GRCh37
NC_000004.10:g.57547455T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314595.6:c.92+106T>C MANE Select	ENSP00000312735.5:n.92+106T>C
ENST00000314595.5:c.92+106T>C	ENSP00000312735.5:n.92+106T>C
ENST00000381227.5:c.92+106T>C	ENSP00000370625.1:n.92+106T>C
ENST00000431623.6:c.18+106T>C	ENSP00000391096.2:n.18+106T>C
ENST00000433463.1:c.71+106T>C	ENSP00000407728.1:n.71+106T>C
ENST00000441246.6:c.71+106T>C	ENSP00000391452.2:n.71+106T>C
ENST00000450656.5:c.92+106T>C	ENSP00000408638.1:n.92+106T>C
ENST00000497845.1:n.280T>C
NM_000938.2:c.92+106T>C	NP_000929.1:n.92+106T>C
NM_001303268.1:c.18+106T>C	NP_001290197.1:n.18+106T>C
NM_001303269.1:c.71+106T>C	NP_001290198.1:n.71+106T>C
NM_000938.3:c.92+106T>C MANE Select	NP_000929.1:n.92+106T>C
NM_001303268.2:c.18+106T>C	NP_001290197.1:n.18+106T>C
NM_001303269.2:c.71+106T>C	NP_001290198.1:n.71+106T>C