Canonical Allele Identifier: CA2736988025

Gene: PCIF1

Linked Data

• dbSNP Id: rs2145343291

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947466A>C , CM000682.2:g.45947466A>C	GRCh38
NC_000020.10:g.44576105A>C , CM000682.1:g.44576105A>C	GRCh37
NC_000020.9:g.44009512A>C	NCBI36
NG_029772.1:g.29729T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.1883+28A>C MANE Select	ENSP00000361486.3:n.1883+28A>C
ENST00000372409.7:c.1883+28A>C	ENSP00000361486.3:n.1883+28A>C
ENST00000479348.2:c.767A>C
NM_022104.3:c.1883+28A>C	NP_071387.1:n.1883+28A>C
XM_011528980.1:c.1883+28A>C	XP_011527282.1:n.1883+28A>C
XM_011528981.1:c.1883+28A>C	XP_011527283.1:n.1883+28A>C
XM_011528982.1:c.839+28A>C	XP_011527284.1:n.839+28A>C
XM_011528980.3:c.1883+28A>C	XP_011527282.1:n.1883+28A>C
XM_011528981.3:c.1883+28A>C	XP_011527283.1:n.1883+28A>C
XM_017028013.2:c.1883+28A>C	XP_016883502.1:n.1883+28A>C
XM_017028014.2:c.839+28A>C	XP_016883503.1:n.839+28A>C
NM_022104.4:c.1883+28A>C MANE Select	NP_071387.1:n.1883+28A>C