Canonical Allele Identifier: CA3825399

Gene: POLR1C

Linked Data

• ClinVar Variation Id: 2417502
• ClinVar RCV Id: RCV003114971
• dbSNP Id: rs780090128
• ExAC: 6:43487481 A / G
• gnomAD v2: 6-43487481-A-G
• gnomAD v3: 6-43519743-A-G
• gnomAD v4: 6-43519743-A-G
• MyVariant Identifiers: chr6:g.43487481A>G (hg19) ; chr6:g.43519743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43519743A>G , CM000668.2:g.43519743A>G	GRCh38
NC_000006.11:g.43487481A>G , CM000668.1:g.43487481A>G	GRCh37
NC_000006.10:g.43595459A>G	NCBI36
NG_028283.1:g.7705A>G
NG_028283.3:g.15042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.287A>G	ENSP00000496683.1:p.Asn96Ser
ENST00000642195.1:c.287A>G MANE Select	ENSP00000496044.1:p.Asn96Ser
ENST00000643341.1:c.287A>G	ENSP00000496018.1:p.Asn96Ser
ENST00000643799.1:c.287A>G	ENSP00000494529.1:p.Asn96Ser
ENST00000645141.1:c.287A>G	ENSP00000496755.1:p.Asn96Ser
ENST00000646188.1:c.122A>G	ENSP00000496001.1:p.Asn41Ser
ENST00000646433.1:c.287A>G	ENSP00000494368.1:p.Asn96Ser
ENST00000646700.1:c.287A>G	ENSP00000495521.1:p.Asn96Ser
ENST00000304004.7:c.287A>G	ENSP00000307212.3:p.Asn96Ser
ENST00000372344.6:c.287A>G	ENSP00000361419.2:p.Asn96Ser
ENST00000372389.7:c.287A>G	ENSP00000361465.3:p.Asn96Ser
ENST00000423780.1:c.285A>G
ENST00000428025.6:c.122A>G	ENSP00000395401.2:p.Asn41Ser
ENST00000455605.2:n.264A>G
ENST00000481352.6:n.343A>G
ENST00000488601.6:n.299A>G
NM_203290.2:c.287A>G	NP_976035.1:p.Asn96Ser
XM_005249491.1:c.287A>G	XP_005249548.1:p.Asn96Ser
XM_011515000.1:c.287A>G	XP_011513302.1:p.Asn96Ser
NM_001318876.1:c.287A>G	NP_001305805.1:p.Asn96Ser
NM_001363658.1:c.287A>G	NP_001350587.1:p.Asn96Ser
NM_203290.3:c.287A>G	NP_976035.1:p.Asn96Ser
NM_203290.4:c.287A>G MANE Select	NP_976035.1:p.Asn96Ser
NM_001363658.2:c.287A>G	NP_001350587.1:p.Asn96Ser
NM_001318876.2:c.287A>G	NP_001305805.1:p.Asn96Ser