Canonical Allele Identifier: CA446894958
Gene: HDAC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.141005700T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626133T>A , CM000667.2:g.141626133T>A GRCh38
NC_000005.9:g.141005700T>A , CM000667.1:g.141005700T>A GRCh37
NC_000005.8:g.140985884T>A NCBI36
NG_029678.1:g.15724A>T
NG_029678.2:g.15724A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.921-62A>T MANE Select ENSP00000302967.3:n.921-62A>T
ENST00000305264.7:c.921-62A>T ENSP00000302967.3:n.921-62A>T
ENST00000459727.5:n.233+61A>T
ENST00000467533.5:n.599+61A>T
ENST00000469550.6:n.994-62A>T
ENST00000475549.1:n.252-62A>T
ENST00000486618.1:n.353A>T
ENST00000491581.5:n.135-62A>T
ENST00000492407.1:n.767+61A>T
NM_003883.3:c.921-62A>T NP_003874.2:n.921-62A>T
XM_011537697.1:c.360-62A>T XP_011535999.1:n.360-62A>T
XR_944336.1:n.1006-62A>T
NM_001355039.1:c.921-62A>T NP_001341968.1:n.921-62A>T
NM_001355040.1:c.462-62A>T NP_001341969.1:n.462-62A>T
NM_001355041.1:c.360-62A>T NP_001341970.1:n.360-62A>T
NR_149164.1:n.987-62A>T
NR_149165.1:n.869-62A>T
NR_149166.1:n.843+61A>T
NR_149167.1:n.1011+61A>T
NR_149168.1:n.1012-62A>T
NR_149169.1:n.1012-62A>T
NM_003883.4:c.921-62A>T MANE Select NP_003874.2:n.921-62A>T
NM_001355039.2:c.921-62A>T NP_001341968.1:n.921-62A>T
NR_149167.2:n.1004+61A>T
NM_001355040.2:c.462-62A>T NP_001341969.1:n.462-62A>T
NM_001355041.2:c.360-62A>T NP_001341970.1:n.360-62A>T
NR_149164.2:n.980-62A>T
NR_149165.2:n.862-62A>T
NR_149166.2:n.836+61A>T
NR_149168.2:n.1005-62A>T
NR_149169.2:n.1005-62A>T