Canonical Allele Identifier: CA771905981

Gene: ZPBP2

Linked Data

• dbSNP Id: rs1374900082
• gnomAD v3: 17-39872148-T-A
• gnomAD v4: 17-39872148-T-A
• MyVariant Identifiers: chr17:g.38028401T>A (hg19) ; chr17:g.39872148T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872148T>A , CM000679.2:g.39872148T>A	GRCh38
NC_000017.10:g.38028401T>A , CM000679.1:g.38028401T>A	GRCh37
NC_000017.9:g.35281927T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-122T>A MANE Select	ENSP00000335384.5:n.407-122T>A
ENST00000348931.8:c.407-122T>A	ENSP00000335384.5:n.407-122T>A
ENST00000377940.3:c.341-122T>A	ENSP00000367174.3:n.341-122T>A
ENST00000583811.5:c.53-122T>A	ENSP00000462463.1:n.53-122T>A
ENST00000584588.5:c.406+523T>A	ENSP00000462067.1:n.406+523T>A
NM_198844.2:c.341-122T>A	NP_942141.2:n.341-122T>A
NM_199321.2:c.407-122T>A	NP_955353.1:n.407-122T>A
XM_011524298.1:c.407-122T>A	XP_011522600.1:n.407-122T>A
XR_002957959.1:n.598-122T>A
NM_198844.3:c.341-122T>A	NP_942141.2:n.341-122T>A
NM_199321.3:c.407-122T>A MANE Select	NP_955353.1:n.407-122T>A