Canonical Allele Identifier: CA8535989

Gene: ZPBP2

Linked Data

• dbSNP Id: rs759618203
• ExAC: 17:38028772 A / C
• gnomAD v2: 17-38028772-A-C
• gnomAD v3: 17-39872519-A-C
• gnomAD v4: 17-39872519-A-C
• MyVariant Identifiers: chr17:g.38028772A>C (hg19) ; chr17:g.39872519A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872519A>C , CM000679.2:g.39872519A>C	GRCh38
NC_000017.10:g.38028772A>C , CM000679.1:g.38028772A>C	GRCh37
NC_000017.9:g.35282298A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+31A>C MANE Select	ENSP00000335384.5:n.625+31A>C
ENST00000348931.8:c.625+31A>C	ENSP00000335384.5:n.625+31A>C
ENST00000377940.3:c.559+31A>C	ENSP00000367174.3:n.559+31A>C
ENST00000583811.5:c.271+31A>C	ENSP00000462463.1:n.271+31A>C
ENST00000584588.5:c.407-525A>C	ENSP00000462067.1:n.407-525A>C
NM_198844.2:c.559+31A>C	NP_942141.2:n.559+31A>C
NM_199321.2:c.625+31A>C	NP_955353.1:n.625+31A>C
XM_011524298.1:c.625+31A>C	XP_011522600.1:n.625+31A>C
XR_002957959.1:n.816+31A>C
NM_198844.3:c.559+31A>C	NP_942141.2:n.559+31A>C
NM_199321.3:c.625+31A>C MANE Select	NP_955353.1:n.625+31A>C