Canonical Allele Identifier: CA371775413
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs1342210101
gnomAD v3: 8-98157636-C-G
gnomAD v4: 8-98157636-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157636C>G , CM000670.2:g.98157636C>G GRCh38
NC_000008.10:g.99169864C>G , CM000670.1:g.99169864C>G GRCh37
NC_000008.9:g.99239040C>G NCBI36
NG_052869.1:g.45344C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2440C>G MANE Select ENSP00000385787.2:p.Gln814Glu
ENST00000349693.3:c.2440C>G ENSP00000339529.3:p.Gln814Glu
ENST00000401707.6:c.2440C>G ENSP00000385787.2:p.Gln814Glu
ENST00000517435.1:n.475C>G
NM_001145860.1:c.2440C>G NP_001139332.1:p.Gln814Glu
NM_001145861.1:c.2440C>G NP_001139333.1:p.Gln814Glu
NM_015029.2:c.2440C>G NP_055844.2:p.Gln814Glu
NM_001145860.2:c.2440C>G MANE Select NP_001139332.1:p.Gln814Glu
NM_001145861.2:c.2440C>G NP_001139333.1:p.Gln814Glu
NM_015029.3:c.2440C>G NP_055844.2:p.Gln814Glu