Canonical Allele Identifier: CA744845196

Gene: PCIF1

Linked Data

• dbSNP Id: rs1264842152
• gnomAD v3: 20-45947762-C-T
• gnomAD v4: 20-45947762-C-T
• MyVariant Identifiers: chr20:g.44576401C>T (hg19) ; chr20:g.45947762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947762C>T , CM000682.2:g.45947762C>T	GRCh38
NC_000020.10:g.44576401C>T , CM000682.1:g.44576401C>T	GRCh37
NC_000020.9:g.44009808C>T	NCBI36
NG_029772.1:g.29433G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*7C>T MANE Select	ENSP00000361486.3:n.*7C>T
ENST00000372409.7:c.*7C>T	ENSP00000361486.3:n.*7C>T
ENST00000479348.2:c.1063C>T
NM_022104.3:c.*7C>T	NP_071387.1:n.*7C>T
XM_011528980.1:c.*7C>T	XP_011527282.1:n.*7C>T
XM_011528981.1:c.*7C>T	XP_011527283.1:n.*7C>T
XM_011528982.1:c.*7C>T	XP_011527284.1:n.*7C>T
XM_011528980.3:c.*7C>T	XP_011527282.1:n.*7C>T
XM_011528981.3:c.*7C>T	XP_011527283.1:n.*7C>T
XM_017028013.2:c.*7C>T	XP_016883502.1:n.*7C>T
XM_017028014.2:c.*7C>T	XP_016883503.1:n.*7C>T
NM_022104.4:c.*7C>T MANE Select	NP_071387.1:n.*7C>T