Canonical Allele Identifier: CA507815877
Gene: POLR1G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45910398A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45407140A>C , CM000681.2:g.45407140A>C GRCh38
NC_000019.9:g.45910398A>C , CM000681.1:g.45910398A>C GRCh37
NC_000019.8:g.50602238A>C NCBI36
NG_015839.2:g.76689T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309424.8:c.69A>C MANE Select ENSP00000310966.3:p.Pro23=
ENST00000309424.7:c.69A>C ENSP00000310966.3:p.Pro23=
ENST00000589804.1:c.75A>C ENSP00000465099.1:p.Pro25=
ENST00000590794.1:c.20+422A>C
ENST00000592852.1:c.-466A>C ENSP00000467771.1:n.-466A>C
NM_001297590.1:c.75A>C NP_001284519.1:p.Pro25=
NM_012099.1:c.69A>C NP_036231.1:p.Pro23=
NM_001297590.2:c.75A>C NP_001284519.1:p.Pro25=
NM_012099.2:c.69A>C NP_036231.1:p.Pro23=
NM_001297590.3:c.75A>C NP_001284519.1:p.Pro25=
NM_012099.3:c.69A>C MANE Select NP_036231.1:p.Pro23=