Canonical Allele Identifier: CA499931742
Gene: ZPBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.38028665A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872412A>C , CM000679.2:g.39872412A>C GRCh38
NC_000017.10:g.38028665A>C , CM000679.1:g.38028665A>C GRCh37
NC_000017.9:g.35282191A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.549A>C MANE Select ENSP00000335384.5:p.Ile183=
ENST00000348931.8:c.549A>C ENSP00000335384.5:p.Ile183=
ENST00000377940.3:c.483A>C ENSP00000367174.3:p.Ile161=
ENST00000583811.5:c.195A>C ENSP00000462463.1:p.Ile65=
ENST00000584588.5:c.407-632A>C ENSP00000462067.1:n.407-632A>C
NM_198844.2:c.483A>C NP_942141.2:p.Ile161=
NM_199321.2:c.549A>C NP_955353.1:p.Ile183=
XM_011524298.1:c.549A>C XP_011522600.1:p.Ile183=
XR_002957959.1:n.740A>C
NM_198844.3:c.483A>C NP_942141.2:p.Ile161=
NM_199321.3:c.549A>C MANE Select NP_955353.1:p.Ile183=