Canonical Allele Identifier: CA308937262

Gene: POLR1G

Linked Data

• dbSNP Id: rs924710620
• gnomAD v4: 19-45406871-G-A
• MyVariant Identifiers: chr19:g.45910129G>A (hg19) ; chr19:g.45406871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45406871G>A , CM000681.2:g.45406871G>A	GRCh38
NC_000019.9:g.45910129G>A , CM000681.1:g.45910129G>A	GRCh37
NC_000019.8:g.50601969G>A	NCBI36
NG_015839.2:g.76958C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309424.8:c.22+153G>A MANE Select	ENSP00000310966.3:n.22+153G>A
ENST00000309424.7:c.22+153G>A	ENSP00000310966.3:n.22+153G>A
ENST00000589804.1:c.28+147G>A	ENSP00000465099.1:n.28+147G>A
ENST00000590794.1:c.20+153G>A
ENST00000592852.1:c.-735G>A	ENSP00000467771.1:n.-735G>A
NM_001297590.1:c.28+147G>A	NP_001284519.1:n.28+147G>A
NM_012099.1:c.22+153G>A	NP_036231.1:n.22+153G>A
NM_001297590.2:c.28+147G>A	NP_001284519.1:n.28+147G>A
NM_012099.2:c.22+153G>A	NP_036231.1:n.22+153G>A
NM_001297590.3:c.28+147G>A	NP_001284519.1:n.28+147G>A
NM_012099.3:c.22+153G>A MANE Select	NP_036231.1:n.22+153G>A