Canonical Allele Identifier: CA636176170

Gene: PCIF1

Linked Data

• dbSNP Id: rs1351138623
• gnomAD v2: 20-44576402-T-A
• gnomAD v4: 20-45947763-T-A
• MyVariant Identifiers: chr20:g.44576402T>A (hg19) ; chr20:g.45947763T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947763T>A , CM000682.2:g.45947763T>A	GRCh38
NC_000020.10:g.44576402T>A , CM000682.1:g.44576402T>A	GRCh37
NC_000020.9:g.44009809T>A	NCBI36
NG_029772.1:g.29432A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.*8T>A MANE Select	ENSP00000361486.3:n.*8T>A
ENST00000372409.7:c.*8T>A	ENSP00000361486.3:n.*8T>A
ENST00000479348.2:c.1064T>A
NM_022104.3:c.*8T>A	NP_071387.1:n.*8T>A
XM_011528980.1:c.*8T>A	XP_011527282.1:n.*8T>A
XM_011528981.1:c.*8T>A	XP_011527283.1:n.*8T>A
XM_011528982.1:c.*8T>A	XP_011527284.1:n.*8T>A
XM_011528980.3:c.*8T>A	XP_011527282.1:n.*8T>A
XM_011528981.3:c.*8T>A	XP_011527283.1:n.*8T>A
XM_017028013.2:c.*8T>A	XP_016883502.1:n.*8T>A
XM_017028014.2:c.*8T>A	XP_016883503.1:n.*8T>A
NM_022104.4:c.*8T>A MANE Select	NP_071387.1:n.*8T>A