Canonical Allele Identifier: CA371775366
Gene: POP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.99169844G>A (hg19) chr8:g.98157616G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157616G>A , CM000670.2:g.98157616G>A GRCh38
NC_000008.10:g.99169844G>A , CM000670.1:g.99169844G>A GRCh37
NC_000008.9:g.99239020G>A NCBI36
NG_052869.1:g.45324G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2421-1G>A MANE Select ENSP00000385787.2:n.2421-1G>A
ENST00000349693.3:c.2421-1G>A ENSP00000339529.3:n.2421-1G>A
ENST00000401707.6:c.2421-1G>A ENSP00000385787.2:n.2421-1G>A
ENST00000517435.1:n.456-1G>A
NM_001145860.1:c.2421-1G>A NP_001139332.1:n.2421-1G>A
NM_001145861.1:c.2421-1G>A NP_001139333.1:n.2421-1G>A
NM_015029.2:c.2421-1G>A NP_055844.2:n.2421-1G>A
NM_001145860.2:c.2421-1G>A MANE Select NP_001139332.1:n.2421-1G>A
NM_001145861.2:c.2421-1G>A NP_001139333.1:n.2421-1G>A
NM_015029.3:c.2421-1G>A NP_055844.2:n.2421-1G>A
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