Canonical Allele Identifier: CA409231335

Gene: PCIF1

Linked Data

• dbSNP Id: rs1600511917
• MyVariant Identifiers: chr20:g.44576261A>G (hg19) ; chr20:g.45947622A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947622A>G , CM000682.2:g.45947622A>G	GRCh38
NC_000020.10:g.44576261A>G , CM000682.1:g.44576261A>G	GRCh37
NC_000020.9:g.44009668A>G	NCBI36
NG_029772.1:g.29573T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.1982A>G MANE Select	ENSP00000361486.3:p.Gln661Arg
ENST00000372409.7:c.1982A>G	ENSP00000361486.3:p.Gln661Arg
ENST00000479348.2:c.923A>G
NM_022104.3:c.1982A>G	NP_071387.1:p.Gln661Arg
XM_011528980.1:c.1982A>G	XP_011527282.1:p.Gln661Arg
XM_011528981.1:c.1982A>G	XP_011527283.1:p.Gln661Arg
XM_011528982.1:c.938A>G	XP_011527284.1:p.Gln313Arg
XM_011528980.3:c.1982A>G	XP_011527282.1:p.Gln661Arg
XM_011528981.3:c.1982A>G	XP_011527283.1:p.Gln661Arg
XM_017028013.2:c.1982A>G	XP_016883502.1:p.Gln661Arg
XM_017028014.2:c.938A>G	XP_016883503.1:p.Gln313Arg
NM_022104.4:c.1982A>G MANE Select	NP_071387.1:p.Gln661Arg