Canonical Allele Identifier: CA2366447762

Gene: PCIF1

Linked Data

• dbSNP Id: rs2083542060
• gnomAD v4: 20-45947479-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947479C>T , CM000682.2:g.45947479C>T	GRCh38
NC_000020.10:g.44576118C>T , CM000682.1:g.44576118C>T	GRCh37
NC_000020.9:g.44009525C>T	NCBI36
NG_029772.1:g.29716G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.1883+41C>T MANE Select	ENSP00000361486.3:n.1883+41C>T
ENST00000372409.7:c.1883+41C>T	ENSP00000361486.3:n.1883+41C>T
ENST00000479348.2:c.780C>T
NM_022104.3:c.1883+41C>T	NP_071387.1:n.1883+41C>T
XM_011528980.1:c.1883+41C>T	XP_011527282.1:n.1883+41C>T
XM_011528981.1:c.1883+41C>T	XP_011527283.1:n.1883+41C>T
XM_011528982.1:c.839+41C>T	XP_011527284.1:n.839+41C>T
XM_011528980.3:c.1883+41C>T	XP_011527282.1:n.1883+41C>T
XM_011528981.3:c.1883+41C>T	XP_011527283.1:n.1883+41C>T
XM_017028013.2:c.1883+41C>T	XP_016883502.1:n.1883+41C>T
XM_017028014.2:c.839+41C>T	XP_016883503.1:n.839+41C>T
NM_022104.4:c.1883+41C>T MANE Select	NP_071387.1:n.1883+41C>T