Canonical Allele Identifier: CA744845224
Gene: PCIF1 HGNC NCBI

Linked Data

dbSNP Id: rs1452201085

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947781C>G , CM000682.2:g.45947781C>G GRCh38
NC_000020.10:g.44576420C>G , CM000682.1:g.44576420C>G GRCh37
NC_000020.9:g.44009827C>G NCBI36
NG_029772.1:g.29414G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*26C>G MANE Select ENSP00000361486.3:n.*26C>G
ENST00000372409.7:c.*26C>G ENSP00000361486.3:n.*26C>G
ENST00000479348.2:c.1082C>G
NM_022104.3:c.*26C>G NP_071387.1:n.*26C>G
XM_011528980.1:c.*26C>G XP_011527282.1:n.*26C>G
XM_011528981.1:c.*26C>G XP_011527283.1:n.*26C>G
XM_011528982.1:c.*26C>G XP_011527284.1:n.*26C>G
XM_011528980.3:c.*26C>G XP_011527282.1:n.*26C>G
XM_011528981.3:c.*26C>G XP_011527283.1:n.*26C>G
XM_017028013.2:c.*26C>G XP_016883502.1:n.*26C>G
XM_017028014.2:c.*26C>G XP_016883503.1:n.*26C>G
NM_022104.4:c.*26C>G MANE Select NP_071387.1:n.*26C>G