Canonical Allele Identifier: CA1116992003
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs1809427921
gnomAD v3: 8-98148658-C-G
gnomAD v4: 8-98148658-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148658C>G , CM000670.2:g.98148658C>G GRCh38
NC_000008.10:g.99160886C>G , CM000670.1:g.99160886C>G GRCh37
NC_000008.9:g.99230062C>G NCBI36
NG_052869.1:g.36366C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-157C>G MANE Select ENSP00000385787.2:n.1711-157C>G
ENST00000349693.3:c.1711-157C>G ENSP00000339529.3:n.1711-157C>G
ENST00000401707.6:c.1711-157C>G ENSP00000385787.2:n.1711-157C>G
NM_001145860.1:c.1711-157C>G NP_001139332.1:n.1711-157C>G
NM_001145861.1:c.1711-157C>G NP_001139333.1:n.1711-157C>G
NM_015029.2:c.1711-157C>G NP_055844.2:n.1711-157C>G
XM_011516800.1:c.1711-157C>G XP_011515102.1:n.1711-157C>G
NM_001145860.2:c.1711-157C>G MANE Select NP_001139332.1:n.1711-157C>G
NM_001145861.2:c.1711-157C>G NP_001139333.1:n.1711-157C>G
NM_015029.3:c.1711-157C>G NP_055844.2:n.1711-157C>G