Canonical Allele Identifier: CA510753665
Gene: PCIF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.44576259G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947620G>T , CM000682.2:g.45947620G>T GRCh38
NC_000020.10:g.44576259G>T , CM000682.1:g.44576259G>T GRCh37
NC_000020.9:g.44009666G>T NCBI36
NG_029772.1:g.29575C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1980G>T MANE Select ENSP00000361486.3:p.Leu660=
ENST00000372409.7:c.1980G>T ENSP00000361486.3:p.Leu660=
ENST00000479348.2:c.921G>T
NM_022104.3:c.1980G>T NP_071387.1:p.Leu660=
XM_011528980.1:c.1980G>T XP_011527282.1:p.Leu660=
XM_011528981.1:c.1980G>T XP_011527283.1:p.Leu660=
XM_011528982.1:c.936G>T XP_011527284.1:p.Leu312=
XM_011528980.3:c.1980G>T XP_011527282.1:p.Leu660=
XM_011528981.3:c.1980G>T XP_011527283.1:p.Leu660=
XM_017028013.2:c.1980G>T XP_016883502.1:p.Leu660=
XM_017028014.2:c.936G>T XP_016883503.1:p.Leu312=
NM_022104.4:c.1980G>T MANE Select NP_071387.1:p.Leu660=