Canonical Allele Identifier: CA507815713
Gene: POLR1G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45910374C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45407116C>T , CM000681.2:g.45407116C>T GRCh38
NC_000019.9:g.45910374C>T , CM000681.1:g.45910374C>T GRCh37
NC_000019.8:g.50602214C>T NCBI36
NG_015839.2:g.76713G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309424.8:c.45C>T MANE Select ENSP00000310966.3:p.Pro15=
ENST00000309424.7:c.45C>T ENSP00000310966.3:p.Pro15=
ENST00000589804.1:c.51C>T ENSP00000465099.1:p.Pro17=
ENST00000590794.1:c.20+398C>T
ENST00000592852.1:c.-490C>T ENSP00000467771.1:n.-490C>T
NM_001297590.1:c.51C>T NP_001284519.1:p.Pro17=
NM_012099.1:c.45C>T NP_036231.1:p.Pro15=
NM_001297590.2:c.51C>T NP_001284519.1:p.Pro17=
NM_012099.2:c.45C>T NP_036231.1:p.Pro15=
NM_001297590.3:c.51C>T NP_001284519.1:p.Pro17=
NM_012099.3:c.45C>T MANE Select NP_036231.1:p.Pro15=