Canonical Allele Identifier: CA882712496

Gene: POLR1G

Linked Data

• dbSNP Id: rs1164555709
• gnomAD v4: 19-45406889-G-A
• MyVariant Identifiers: chr19:g.45910147G>A (hg19) ; chr19:g.45406889G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45406889G>A , CM000681.2:g.45406889G>A	GRCh38
NC_000019.9:g.45910147G>A , CM000681.1:g.45910147G>A	GRCh37
NC_000019.8:g.50601987G>A	NCBI36
NG_015839.2:g.76940C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309424.8:c.22+171G>A MANE Select	ENSP00000310966.3:n.22+171G>A
ENST00000309424.7:c.22+171G>A	ENSP00000310966.3:n.22+171G>A
ENST00000589804.1:c.28+165G>A	ENSP00000465099.1:n.28+165G>A
ENST00000590794.1:c.20+171G>A
ENST00000592852.1:c.-717G>A	ENSP00000467771.1:n.-717G>A
NM_001297590.1:c.28+165G>A	NP_001284519.1:n.28+165G>A
NM_012099.1:c.22+171G>A	NP_036231.1:n.22+171G>A
NM_001297590.2:c.28+165G>A	NP_001284519.1:n.28+165G>A
NM_012099.2:c.22+171G>A	NP_036231.1:n.22+171G>A
NM_001297590.3:c.28+165G>A	NP_001284519.1:n.28+165G>A
NM_012099.3:c.22+171G>A MANE Select	NP_036231.1:n.22+171G>A