Canonical Allele Identifier: CA146143447

Gene: HDAC2

Linked Data

• dbSNP Id: rs10499080
• gnomAD v2: 6-114273646-C-T
• gnomAD v3: 6-113952482-C-T
• gnomAD v4: 6-113952482-C-T
• MyVariant Identifiers: chr6:g.114273646C>T (hg19) ; chr6:g.113952482C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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