Canonical Allele Identifier: CA394621371

Gene: ZNF500

Linked Data

• dbSNP Id: rs771842613
• gnomAD v3: 16-4762755-C-A
• gnomAD v4: 16-4762755-C-A
• MyVariant Identifiers: chr16:g.4812756C>A (hg19) ; chr16:g.4762755C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762755C>A , CM000678.2:g.4762755C>A	GRCh38
NC_000016.9:g.4812756C>A , CM000678.1:g.4812756C>A	GRCh37
NC_000016.8:g.4752757C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.416G>T MANE Select	ENSP00000219478.5:p.Gly139Val
ENST00000219478.10:c.416G>T	ENSP00000219478.5:p.Gly139Val
ENST00000545009.1:c.416G>T	ENSP00000445714.1:p.Gly139Val
ENST00000589422.1:c.415-42G>T	ENSP00000466375.1:n.415-42G>T
NM_001303450.1:c.416G>T	NP_001290379.1:p.Gly139Val
NM_021646.2:c.416G>T	NP_067678.1:p.Gly139Val
XM_005255243.2:c.65G>T	XP_005255300.1:p.Gly22Val
XM_011522453.1:c.416G>T	XP_011520755.1:p.Gly139Val
XM_011522454.1:c.-167-42G>T	XP_011520756.1:n.-167-42G>T
NM_021646.3:c.416G>T	NP_067678.1:p.Gly139Val
XM_005255243.4:c.65G>T	XP_005255300.1:p.Gly22Val
XM_011522453.2:c.416G>T	XP_011520755.1:p.Gly139Val
XM_011522454.3:c.-167-42G>T	XP_011520756.1:n.-167-42G>T
XM_017023121.2:c.-209G>T	XP_016878610.1:n.-209G>T
NM_001303450.2:c.416G>T	NP_001290379.1:p.Gly139Val
NM_021646.4:c.416G>T MANE Select	NP_067678.1:p.Gly139Val