Canonical Allele Identifier: CA499931619
Gene: ZPBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.38028572A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872319A>T , CM000679.2:g.39872319A>T GRCh38
NC_000017.10:g.38028572A>T , CM000679.1:g.38028572A>T GRCh37
NC_000017.9:g.35282098A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.456A>T MANE Select ENSP00000335384.5:p.Thr152=
ENST00000348931.8:c.456A>T ENSP00000335384.5:p.Thr152=
ENST00000377940.3:c.390A>T ENSP00000367174.3:p.Thr130=
ENST00000583811.5:c.102A>T ENSP00000462463.1:p.Thr34=
ENST00000584588.5:c.406+694A>T ENSP00000462067.1:n.406+694A>T
NM_198844.2:c.390A>T NP_942141.2:p.Thr130=
NM_199321.2:c.456A>T NP_955353.1:p.Thr152=
XM_011524298.1:c.456A>T XP_011522600.1:p.Thr152=
XR_002957959.1:n.647A>T
NM_198844.3:c.390A>T NP_942141.2:p.Thr130=
NM_199321.3:c.456A>T MANE Select NP_955353.1:p.Thr152=