Canonical Allele Identifier: CA8535940

Gene: ZPBP2

Linked Data

• dbSNP Id: rs34523816
• ExAC: 17:38028478 C / G
• gnomAD v2: 17-38028478-C-G
• gnomAD v3: 17-39872225-C-G
• gnomAD v4: 17-39872225-C-G
• MyVariant Identifiers: chr17:g.38028478C>G (hg19) ; chr17:g.39872225C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872225C>G , CM000679.2:g.39872225C>G	GRCh38
NC_000017.10:g.38028478C>G , CM000679.1:g.38028478C>G	GRCh37
NC_000017.9:g.35282004C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-45C>G MANE Select	ENSP00000335384.5:n.407-45C>G
ENST00000348931.8:c.407-45C>G	ENSP00000335384.5:n.407-45C>G
ENST00000377940.3:c.341-45C>G	ENSP00000367174.3:n.341-45C>G
ENST00000583811.5:c.53-45C>G	ENSP00000462463.1:n.53-45C>G
ENST00000584588.5:c.406+600C>G	ENSP00000462067.1:n.406+600C>G
NM_198844.2:c.341-45C>G	NP_942141.2:n.341-45C>G
NM_199321.2:c.407-45C>G	NP_955353.1:n.407-45C>G
XM_011524298.1:c.407-45C>G	XP_011522600.1:n.407-45C>G
XR_002957959.1:n.598-45C>G
NM_198844.3:c.341-45C>G	NP_942141.2:n.341-45C>G
NM_199321.3:c.407-45C>G MANE Select	NP_955353.1:n.407-45C>G