Canonical Allele Identifier: CA409231156
Gene: PCIF1 HGNC NCBI

Linked Data

dbSNP Id: rs2083543107

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947538A>C , CM000682.2:g.45947538A>C GRCh38
NC_000020.10:g.44576177A>C , CM000682.1:g.44576177A>C GRCh37
NC_000020.9:g.44009584A>C NCBI36
NG_029772.1:g.29657T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1898A>C MANE Select ENSP00000361486.3:p.Tyr633Ser
ENST00000372409.7:c.1898A>C ENSP00000361486.3:p.Tyr633Ser
ENST00000479348.2:c.839A>C
NM_022104.3:c.1898A>C NP_071387.1:p.Tyr633Ser
XM_011528980.1:c.1898A>C XP_011527282.1:p.Tyr633Ser
XM_011528981.1:c.1898A>C XP_011527283.1:p.Tyr633Ser
XM_011528982.1:c.854A>C XP_011527284.1:p.Tyr285Ser
XM_011528980.3:c.1898A>C XP_011527282.1:p.Tyr633Ser
XM_011528981.3:c.1898A>C XP_011527283.1:p.Tyr633Ser
XM_017028013.2:c.1898A>C XP_016883502.1:p.Tyr633Ser
XM_017028014.2:c.854A>C XP_016883503.1:p.Tyr285Ser
NM_022104.4:c.1898A>C MANE Select NP_071387.1:p.Tyr633Ser