Canonical Allele Identifier: CA386390692
Gene: POLR3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.106857273A>C (hg19) chr12:g.106463495A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.106463495A>C , CM000674.2:g.106463495A>C GRCh38
NC_000012.11:g.106857273A>C , CM000674.1:g.106857273A>C GRCh37
NC_000012.10:g.105381403A>C NCBI36
NG_031837.1:g.110838A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000228347.9:c.2588A>C MANE Select ENSP00000228347.4:p.Asp863Ala
ENST00000228347.8:c.2588A>C ENSP00000228347.4:p.Asp863Ala
ENST00000539066.5:c.2414A>C ENSP00000445721.1:p.Asp805Ala
NM_001160708.1:c.2414A>C NP_001154180.1:p.Asp805Ala
NM_018082.5:c.2588A>C NP_060552.4:p.Asp863Ala
XM_017019621.2:c.2588A>C XP_016875110.1:p.Asp863Ala
NM_018082.6:c.2588A>C MANE Select NP_060552.4:p.Asp863Ala
NM_001160708.2:c.2414A>C NP_001154180.1:p.Asp805Ala
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