Canonical Allele Identifier: CA499931772
Gene: ZPBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.38028710C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872457C>A , CM000679.2:g.39872457C>A GRCh38
NC_000017.10:g.38028710C>A , CM000679.1:g.38028710C>A GRCh37
NC_000017.9:g.35282236C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.594C>A MANE Select ENSP00000335384.5:p.Gly198=
ENST00000348931.8:c.594C>A ENSP00000335384.5:p.Gly198=
ENST00000377940.3:c.528C>A ENSP00000367174.3:p.Gly176=
ENST00000583811.5:c.240C>A ENSP00000462463.1:p.Gly80=
ENST00000584588.5:c.407-587C>A ENSP00000462067.1:n.407-587C>A
NM_198844.2:c.528C>A NP_942141.2:p.Gly176=
NM_199321.2:c.594C>A NP_955353.1:p.Gly198=
XM_011524298.1:c.594C>A XP_011522600.1:p.Gly198=
XR_002957959.1:n.785C>A
NM_198844.3:c.528C>A NP_942141.2:p.Gly176=
NM_199321.3:c.594C>A MANE Select NP_955353.1:p.Gly198=