Canonical Allele Identifier: CA371777553
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs750621809
gnomAD v4: 8-98158063-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158063C>A , CM000670.2:g.98158063C>A GRCh38
NC_000008.10:g.99170291C>A , CM000670.1:g.99170291C>A GRCh37
NC_000008.9:g.99239467C>A NCBI36
NG_052869.1:g.45771C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2867C>A MANE Select ENSP00000385787.2:p.Thr956Lys
ENST00000349693.3:c.2867C>A ENSP00000339529.3:p.Thr956Lys
ENST00000401707.6:c.2867C>A ENSP00000385787.2:p.Thr956Lys
NM_001145860.1:c.2867C>A NP_001139332.1:p.Thr956Lys
NM_001145861.1:c.2867C>A NP_001139333.1:p.Thr956Lys
NM_015029.2:c.2867C>A NP_055844.2:p.Thr956Lys
NM_001145860.2:c.2867C>A MANE Select NP_001139332.1:p.Thr956Lys
NM_001145861.2:c.2867C>A NP_001139333.1:p.Thr956Lys
NM_015029.3:c.2867C>A NP_055844.2:p.Thr956Lys