Canonical Allele Identifier: CA507816466
Gene: POLR1G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45910485C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45407227C>A , CM000681.2:g.45407227C>A GRCh38
NC_000019.9:g.45910485C>A , CM000681.1:g.45910485C>A GRCh37
NC_000019.8:g.50602325C>A NCBI36
NG_015839.2:g.76602G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309424.8:c.156C>A MANE Select ENSP00000310966.3:p.Ala52=
ENST00000309424.7:c.156C>A ENSP00000310966.3:p.Ala52=
ENST00000589804.1:c.162C>A ENSP00000465099.1:p.Ala54=
ENST00000590794.1:c.20+509C>A
ENST00000592852.1:c.-379C>A ENSP00000467771.1:n.-379C>A
NM_001297590.1:c.162C>A NP_001284519.1:p.Ala54=
NM_012099.1:c.156C>A NP_036231.1:p.Ala52=
NM_001297590.2:c.162C>A NP_001284519.1:p.Ala54=
NM_012099.2:c.156C>A NP_036231.1:p.Ala52=
NM_001297590.3:c.162C>A NP_001284519.1:p.Ala54=
NM_012099.3:c.156C>A MANE Select NP_036231.1:p.Ala52=