Canonical Allele Identifier: CA8535985
Gene: ZPBP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2346032
ClinVar RCV Id: RCV004184440
dbSNP Id: rs145761179

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872478A>G , CM000679.2:g.39872478A>G GRCh38
NC_000017.10:g.38028731A>G , CM000679.1:g.38028731A>G GRCh37
NC_000017.9:g.35282257A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.615A>G MANE Select ENSP00000335384.5:p.Ile205Met
ENST00000348931.8:c.615A>G ENSP00000335384.5:p.Ile205Met
ENST00000377940.3:c.549A>G ENSP00000367174.3:p.Ile183Met
ENST00000583811.5:c.261A>G ENSP00000462463.1:p.Ile87Met
ENST00000584588.5:c.407-566A>G ENSP00000462067.1:n.407-566A>G
NM_198844.2:c.549A>G NP_942141.2:p.Ile183Met
NM_199321.2:c.615A>G NP_955353.1:p.Ile205Met
XM_011524298.1:c.615A>G XP_011522600.1:p.Ile205Met
XR_002957959.1:n.806A>G
NM_198844.3:c.549A>G NP_942141.2:p.Ile183Met
NM_199321.3:c.615A>G MANE Select NP_955353.1:p.Ile205Met