Canonical Allele Identifier: CA371778720
Gene: POP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.99170450C>A (hg19) chr8:g.98158222C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158222C>A , CM000670.2:g.98158222C>A GRCh38
NC_000008.10:g.99170450C>A , CM000670.1:g.99170450C>A GRCh37
NC_000008.9:g.99239626C>A NCBI36
NG_052869.1:g.45930C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.3026C>A MANE Select ENSP00000385787.2:p.Pro1009His
ENST00000349693.3:c.3026C>A ENSP00000339529.3:p.Pro1009His
ENST00000401707.6:c.3026C>A ENSP00000385787.2:p.Pro1009His
NM_001145860.1:c.3026C>A NP_001139332.1:p.Pro1009His
NM_001145861.1:c.3026C>A NP_001139333.1:p.Pro1009His
NM_015029.2:c.3026C>A NP_055844.2:p.Pro1009His
NM_001145860.2:c.3026C>A MANE Select NP_001139332.1:p.Pro1009His
NM_001145861.2:c.3026C>A NP_001139333.1:p.Pro1009His
NM_015029.3:c.3026C>A NP_055844.2:p.Pro1009His
Search 100 bp 5'
Search 100 bp 3'