Canonical Allele Identifier: CA1587281971

Gene: HDAC3

Linked Data

• dbSNP Id: rs2099904225
• gnomAD v4: 5-141624770-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624770G>C , CM000667.2:g.141624770G>C	GRCh38
NC_000005.9:g.141004337G>C , CM000667.1:g.141004337G>C	GRCh37
NC_000005.8:g.140984521G>C	NCBI36
NG_029678.1:g.17087C>G
NG_029678.2:g.17087C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305264.8:c.1217+438C>G MANE Select	ENSP00000302967.3:n.1217+438C>G
ENST00000305264.7:c.1217+438C>G	ENSP00000302967.3:n.1217+438C>G
ENST00000459727.5:n.471+438C>G
ENST00000469207.5:n.216+438C>G
ENST00000469550.6:n.1290+438C>G
NM_003883.3:c.1217+438C>G	NP_003874.2:n.1217+438C>G
XM_011537697.1:c.656+438C>G	XP_011535999.1:n.656+438C>G
XR_427789.2:n.231-1077G>C
XR_944336.1:n.1302+438C>G
NM_001355040.1:c.758+438C>G	NP_001341969.1:n.758+438C>G
NM_001355041.1:c.656+438C>G	NP_001341970.1:n.656+438C>G
NR_149164.1:n.1203+438C>G
NR_149165.1:n.1165+438C>G
NR_149166.1:n.1081+438C>G
NR_149168.1:n.1308+438C>G
NR_149169.1:n.1228+438C>G
NM_003883.4:c.1217+438C>G MANE Select	NP_003874.2:n.1217+438C>G
NM_001355040.2:c.758+438C>G	NP_001341969.1:n.758+438C>G
NM_001355041.2:c.656+438C>G	NP_001341970.1:n.656+438C>G
NR_149164.2:n.1196+438C>G
NR_149165.2:n.1158+438C>G
NR_149166.2:n.1074+438C>G
NR_149168.2:n.1301+438C>G
NR_149169.2:n.1221+438C>G