Canonical Allele Identifier: CA210182889

Gene: POLR3A

Linked Data

• dbSNP Id: rs774751433
• gnomAD v2: 10-79735573-G-A
• gnomAD v3: 10-77975815-G-A
• gnomAD v4: 10-77975815-G-A
• MyVariant Identifiers: chr10:g.79735573G>A (hg19) ; chr10:g.77975815G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975815G>A , CM000672.2:g.77975815G>A	GRCh38
NC_000010.10:g.79735573G>A , CM000672.1:g.79735573G>A	GRCh37
NC_000010.9:g.79405579G>A	NCBI36
NG_029648.1:g.58726C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4326C>T
ENST00000698725.1:n.3506C>T
ENST00000698726.1:n.5066C>T
ENST00000698727.1:n.4799C>T
ENST00000698728.1:n.5415C>T
ENST00000698729.1:n.6863C>T
ENST00000698730.1:n.6961C>T
ENST00000698731.1:c.*1663C>T	ENSP00000513898.1:n.*1663C>T
ENST00000698732.1:c.*4525C>T	ENSP00000513899.1:n.*4525C>T
ENST00000698733.1:c.*5023C>T	ENSP00000513900.1:n.*5023C>T
ENST00000698734.1:c.*4009C>T	ENSP00000513901.1:n.*4009C>T
ENST00000698735.1:n.6187C>T
ENST00000698736.1:n.6600C>T
ENST00000372371.8:c.*1663C>T MANE Select	ENSP00000361446.3:n.*1663C>T
ENST00000372371.7:c.*1663C>T	ENSP00000361446.3:n.*1663C>T
ENST00000616246.4:c.472+4326C>T	ENSP00000483738.1:n.472+4326C>T
NM_007055.3:c.*1663C>T	NP_008986.2:n.*1663C>T
NM_007055.4:c.*1663C>T MANE Select	NP_008986.2:n.*1663C>T