Canonical Allele Identifier: CA462457509
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs1278353520
gnomAD v3: 8-98158133-A-G
gnomAD v4: 8-98158133-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158133A>G , CM000670.2:g.98158133A>G GRCh38
NC_000008.10:g.99170361A>G , CM000670.1:g.99170361A>G GRCh37
NC_000008.9:g.99239537A>G NCBI36
NG_052869.1:g.45841A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2937A>G MANE Select ENSP00000385787.2:p.Gly979=
ENST00000349693.3:c.2937A>G ENSP00000339529.3:p.Gly979=
ENST00000401707.6:c.2937A>G ENSP00000385787.2:p.Gly979=
NM_001145860.1:c.2937A>G NP_001139332.1:p.Gly979=
NM_001145861.1:c.2937A>G NP_001139333.1:p.Gly979=
NM_015029.2:c.2937A>G NP_055844.2:p.Gly979=
NM_001145860.2:c.2937A>G MANE Select NP_001139332.1:p.Gly979=
NM_001145861.2:c.2937A>G NP_001139333.1:p.Gly979=
NM_015029.3:c.2937A>G NP_055844.2:p.Gly979=