Canonical Allele Identifier: CA4820848
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs770005409
gnomAD v2: 8-99169879-T-A
gnomAD v3: 8-98157651-T-A
gnomAD v4: 8-98157651-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157651T>A , CM000670.2:g.98157651T>A GRCh38
NC_000008.10:g.99169879T>A , CM000670.1:g.99169879T>A GRCh37
NC_000008.9:g.99239055T>A NCBI36
NG_052869.1:g.45359T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2455T>A MANE Select ENSP00000385787.2:p.Cys819Ser
ENST00000349693.3:c.2455T>A ENSP00000339529.3:p.Cys819Ser
ENST00000401707.6:c.2455T>A ENSP00000385787.2:p.Cys819Ser
ENST00000517435.1:n.490T>A
NM_001145860.1:c.2455T>A NP_001139332.1:p.Cys819Ser
NM_001145861.1:c.2455T>A NP_001139333.1:p.Cys819Ser
NM_015029.2:c.2455T>A NP_055844.2:p.Cys819Ser
NM_001145860.2:c.2455T>A MANE Select NP_001139332.1:p.Cys819Ser
NM_001145861.2:c.2455T>A NP_001139333.1:p.Cys819Ser
NM_015029.3:c.2455T>A NP_055844.2:p.Cys819Ser