Canonical Allele Identifier: CA2366447942
Gene: PCIF1 HGNC NCBI

Linked Data

dbSNP Id: rs752842439

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947786G>C , CM000682.2:g.45947786G>C GRCh38
NC_000020.10:g.44576425G>C , CM000682.1:g.44576425G>C GRCh37
NC_000020.9:g.44009832G>C NCBI36
NG_029772.1:g.29409C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*31G>C MANE Select ENSP00000361486.3:n.*31G>C
ENST00000372409.7:c.*31G>C ENSP00000361486.3:n.*31G>C
ENST00000479348.2:c.1087G>C
NM_022104.3:c.*31G>C NP_071387.1:n.*31G>C
XM_011528980.1:c.*31G>C XP_011527282.1:n.*31G>C
XM_011528981.1:c.*31G>C XP_011527283.1:n.*31G>C
XM_011528982.1:c.*31G>C XP_011527284.1:n.*31G>C
XM_011528980.3:c.*31G>C XP_011527282.1:n.*31G>C
XM_011528981.3:c.*31G>C XP_011527283.1:n.*31G>C
XM_017028013.2:c.*31G>C XP_016883502.1:n.*31G>C
XM_017028014.2:c.*31G>C XP_016883503.1:n.*31G>C
NM_022104.4:c.*31G>C MANE Select NP_071387.1:n.*31G>C