Canonical Allele Identifier: CA499931761
Gene: ZPBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.38028692T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872439T>G , CM000679.2:g.39872439T>G GRCh38
NC_000017.10:g.38028692T>G , CM000679.1:g.38028692T>G GRCh37
NC_000017.9:g.35282218T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.576T>G MANE Select ENSP00000335384.5:p.Val192=
ENST00000348931.8:c.576T>G ENSP00000335384.5:p.Val192=
ENST00000377940.3:c.510T>G ENSP00000367174.3:p.Val170=
ENST00000583811.5:c.222T>G ENSP00000462463.1:p.Val74=
ENST00000584588.5:c.407-605T>G ENSP00000462067.1:n.407-605T>G
NM_198844.2:c.510T>G NP_942141.2:p.Val170=
NM_199321.2:c.576T>G NP_955353.1:p.Val192=
XM_011524298.1:c.576T>G XP_011522600.1:p.Val192=
XR_002957959.1:n.767T>G
NM_198844.3:c.510T>G NP_942141.2:p.Val170=
NM_199321.3:c.576T>G MANE Select NP_955353.1:p.Val192=