Canonical Allele Identifier: CA620716795
Gene: ZNF500 HGNC NCBI

Linked Data

dbSNP Id: rs1477855903
gnomAD v2: 16-4812380-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762379T>C , CM000678.2:g.4762379T>C GRCh38
NC_000016.9:g.4812380T>C , CM000678.1:g.4812380T>C GRCh37
NC_000016.8:g.4752381T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.599-44A>G MANE Select ENSP00000219478.5:n.599-44A>G
ENST00000219478.10:c.599-44A>G ENSP00000219478.5:n.599-44A>G
ENST00000545009.1:c.599-44A>G ENSP00000445714.1:n.599-44A>G
ENST00000589422.1:c.*127-44A>G ENSP00000466375.1:n.*127-44A>G
NM_001303450.1:c.599-44A>G NP_001290379.1:n.599-44A>G
NM_021646.2:c.599-44A>G NP_067678.1:n.599-44A>G
XM_005255243.2:c.248-44A>G XP_005255300.1:n.248-44A>G
XM_011522453.1:c.599-44A>G XP_011520755.1:n.599-44A>G
XM_011522454.1:c.-26-44A>G XP_011520756.1:n.-26-44A>G
NM_021646.3:c.599-44A>G NP_067678.1:n.599-44A>G
XM_005255243.4:c.248-44A>G XP_005255300.1:n.248-44A>G
XM_011522453.2:c.599-44A>G XP_011520755.1:n.599-44A>G
XM_011522454.3:c.-26-44A>G XP_011520756.1:n.-26-44A>G
XM_017023121.2:c.-26-44A>G XP_016878610.1:n.-26-44A>G
NM_001303450.2:c.599-44A>G NP_001290379.1:n.599-44A>G
NM_021646.4:c.599-44A>G MANE Select NP_067678.1:n.599-44A>G