Canonical Allele Identifier: CA507815665
Gene: POLR1G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45910368T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45407110T>C , CM000681.2:g.45407110T>C GRCh38
NC_000019.9:g.45910368T>C , CM000681.1:g.45910368T>C GRCh37
NC_000019.8:g.50602208T>C NCBI36
NG_015839.2:g.76719A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309424.8:c.39T>C MANE Select ENSP00000310966.3:p.Ser13=
ENST00000309424.7:c.39T>C ENSP00000310966.3:p.Ser13=
ENST00000589804.1:c.45T>C ENSP00000465099.1:p.Ser15=
ENST00000590794.1:c.20+392T>C
ENST00000592852.1:c.-496T>C ENSP00000467771.1:n.-496T>C
NM_001297590.1:c.45T>C NP_001284519.1:p.Ser15=
NM_012099.1:c.39T>C NP_036231.1:p.Ser13=
NM_001297590.2:c.45T>C NP_001284519.1:p.Ser15=
NM_012099.2:c.39T>C NP_036231.1:p.Ser13=
NM_001297590.3:c.45T>C NP_001284519.1:p.Ser15=
NM_012099.3:c.39T>C MANE Select NP_036231.1:p.Ser13=