Canonical Allele Identifier: CA1805111331
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs1809431582
gnomAD v4: 8-98148721-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148721G>A , CM000670.2:g.98148721G>A GRCh38
NC_000008.10:g.99160949G>A , CM000670.1:g.99160949G>A GRCh37
NC_000008.9:g.99230125G>A NCBI36
NG_052869.1:g.36429G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-94G>A MANE Select ENSP00000385787.2:n.1711-94G>A
ENST00000349693.3:c.1711-94G>A ENSP00000339529.3:n.1711-94G>A
ENST00000401707.6:c.1711-94G>A ENSP00000385787.2:n.1711-94G>A
NM_001145860.1:c.1711-94G>A NP_001139332.1:n.1711-94G>A
NM_001145861.1:c.1711-94G>A NP_001139333.1:n.1711-94G>A
NM_015029.2:c.1711-94G>A NP_055844.2:n.1711-94G>A
XM_011516800.1:c.1711-94G>A XP_011515102.1:n.1711-94G>A
NM_001145860.2:c.1711-94G>A MANE Select NP_001139332.1:n.1711-94G>A
NM_001145861.2:c.1711-94G>A NP_001139333.1:n.1711-94G>A
NM_015029.3:c.1711-94G>A NP_055844.2:n.1711-94G>A