Canonical Allele Identifier: CA12415977

Gene: HDAC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.113949764C>T , CM000668.2:g.113949764C>T	GRCh38
NC_000006.11:g.114270928C>T , CM000668.1:g.114270928C>T	GRCh37
NC_000006.10:g.114377621C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519065.6:c.640-504G>A MANE Select	ENSP00000430432.1:n.640-504G>A
ENST00000368632.6:c.550-504G>A	ENSP00000357621.2:n.550-504G>A
ENST00000519065.5:c.640-504G>A	ENSP00000430432.1:n.640-504G>A
ENST00000519108.5:c.550-504G>A	ENSP00000430008.1:n.550-504G>A
ENST00000523334.1:n.733-504G>A
NM_001527.3:c.640-504G>A	NP_001518.3:n.640-504G>A
NR_033441.1:n.955-504G>A
NR_073443.1:n.833-504G>A
XM_011535786.1:c.640-504G>A	XP_011534088.1:n.640-504G>A
XM_011535787.1:c.550-504G>A	XP_011534089.1:n.550-504G>A
XM_011535788.1:c.550-504G>A	XP_011534090.1:n.550-504G>A
XM_017010799.1:c.550-504G>A	XP_016866288.1:n.550-504G>A
NM_001527.4:c.640-504G>A MANE Select	NP_001518.3:n.640-504G>A
NR_033441.2:n.908-504G>A
NR_073443.2:n.838-504G>A