Canonical Allele Identifier: CA15593372
Gene: ZNF510 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10816533

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96776856G>C , CM000671.2:g.96776856G>C GRCh38
NC_000009.10:g.98578959G>C NCBI36
NC_000009.11:g.99539138G>C , CM000671.1:g.99539138G>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000223428.8:c.-176-611C>G ENSP00000223428.4:p.=
ENST00000374641.3:c.-176-611C>G ENSP00000363772.3:p.=
ENST00000375231.5:c.-176-611C>G ENSP00000364379.1:p.=
NM_001314059.1:c.-176-611C>G VV NP_001300988.1:p.=
NM_001314060.1:c.-303-611C>G VV NP_001300989.1:p.=
NM_014930.1:c.-176-611C>G VV
NM_014930.2:c.-176-611C>G VV NP_055745.1:p.=
XM_005251807.2:c.-176-611C>G XP_005251864.1:p.=
XM_005251808.2:c.-176-611C>G XP_005251865.1:p.=
XM_005251809.2:c.-303-611C>G XP_005251866.1:p.=
XM_011518393.2:c.-387-611C>G
XM_017014483.1:c.-176-611C>G XP_016869972.1:p.=