Canonical Allele Identifier: CA2717998778
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs2130623110
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148481T>G , CM000670.2:g.98148481T>G GRCh38
NC_000008.10:g.99160709T>G , CM000670.1:g.99160709T>G GRCh37
NC_000008.9:g.99229885T>G NCBI36
NG_052869.1:g.36189T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-334T>G MANE Select ENSP00000385787.2:n.1711-334T>G
ENST00000349693.3:c.1711-334T>G ENSP00000339529.3:n.1711-334T>G
ENST00000401707.6:c.1711-334T>G ENSP00000385787.2:n.1711-334T>G
NM_001145860.1:c.1711-334T>G NP_001139332.1:n.1711-334T>G
NM_001145861.1:c.1711-334T>G NP_001139333.1:n.1711-334T>G
NM_015029.2:c.1711-334T>G NP_055844.2:n.1711-334T>G
XM_011516800.1:c.1711-334T>G XP_011515102.1:n.1711-334T>G
NM_001145860.2:c.1711-334T>G MANE Select NP_001139332.1:n.1711-334T>G
NM_001145861.2:c.1711-334T>G NP_001139333.1:n.1711-334T>G
NM_015029.3:c.1711-334T>G NP_055844.2:n.1711-334T>G
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