Canonical Allele Identifier: CA7881521

Gene: ZNF500

Linked Data

• dbSNP Id: rs201888102
• ExAC: 16:4812796 G / T
• gnomAD v2: 16-4812796-G-T
• gnomAD v3: 16-4762795-G-T
• gnomAD v4: 16-4762795-G-T
• MyVariant Identifiers: chr16:g.4812796G>T (hg19) ; chr16:g.4762795G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762795G>T , CM000678.2:g.4762795G>T	GRCh38
NC_000016.9:g.4812796G>T , CM000678.1:g.4812796G>T	GRCh37
NC_000016.8:g.4752797G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-39C>A MANE Select	ENSP00000219478.5:n.415-39C>A
ENST00000219478.10:c.415-39C>A	ENSP00000219478.5:n.415-39C>A
ENST00000545009.1:c.415-39C>A	ENSP00000445714.1:n.415-39C>A
ENST00000589422.1:c.415-82C>A	ENSP00000466375.1:n.415-82C>A
NM_001303450.1:c.415-39C>A	NP_001290379.1:n.415-39C>A
NM_021646.2:c.415-39C>A	NP_067678.1:n.415-39C>A
XM_005255243.2:c.64-39C>A	XP_005255300.1:n.64-39C>A
XM_011522453.1:c.415-39C>A	XP_011520755.1:n.415-39C>A
XM_011522454.1:c.-167-82C>A	XP_011520756.1:n.-167-82C>A
NM_021646.3:c.415-39C>A	NP_067678.1:n.415-39C>A
XM_005255243.4:c.64-39C>A	XP_005255300.1:n.64-39C>A
XM_011522453.2:c.415-39C>A	XP_011520755.1:n.415-39C>A
XM_011522454.3:c.-167-82C>A	XP_011520756.1:n.-167-82C>A
XM_017023121.2:c.-210-39C>A	XP_016878610.1:n.-210-39C>A
NM_001303450.2:c.415-39C>A	NP_001290379.1:n.415-39C>A
NM_021646.4:c.415-39C>A MANE Select	NP_067678.1:n.415-39C>A