Canonical Allele Identifier: CA1656080012
Gene: HDAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.113952482C= , CM000668.2:g.113952482C= GRCh38
NC_000006.11:g.114273646C= , CM000668.1:g.114273646C= GRCh37
NC_000006.10:g.114380339C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000519065.6:c.639+795G= MANE Select ENSP00000430432.1:n.639+795G=
ENST00000368632.6:c.549+795G= ENSP00000357621.2:n.549+795G=
ENST00000519065.5:c.639+795G= ENSP00000430432.1:n.639+795G=
ENST00000519108.5:c.549+795G= ENSP00000430008.1:n.549+795G=
ENST00000523334.1:n.732+795G=
NM_001527.3:c.639+795G= NP_001518.3:n.639+795G=
NR_033441.1:n.954+795G=
NR_073443.1:n.832+795G=
XM_011535786.1:c.639+795G= XP_011534088.1:n.639+795G=
XM_011535787.1:c.549+795G= XP_011534089.1:n.549+795G=
XM_011535788.1:c.549+795G= XP_011534090.1:n.549+795G=
XM_017010799.1:c.549+795G= XP_016866288.1:n.549+795G=
NM_001527.4:c.639+795G= MANE Select NP_001518.3:n.639+795G=
NR_033441.2:n.907+795G=
NR_073443.2:n.837+795G=