Canonical Allele Identifier: CA7702051

Gene: HOMER2

Linked Data

• ClinVar Variation Id: 1267704
• ClinVar RCV Id: RCV001678257
• dbSNP Id: rs1256429
• ExAC: 15:83521036 C / T
• gnomAD v2: 15-83521036-C-T
• gnomAD v3: 15-82852284-C-T
• gnomAD v4: 15-82852284-C-T
• MyVariant Identifiers: chr15:g.83521036C>T (hg19) ; chr15:g.82852284C>T (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82852284C>T , CM000677.2:g.82852284C>T	GRCh38
NC_000015.9:g.83521036C>T , CM000677.1:g.83521036C>T	GRCh37
NC_000015.8:g.81318090C>T	NCBI36
NG_029435.1:g.105441G>A
NG_029435.2:g.105441G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450735.7:c.652-32G>A MANE Select	ENSP00000407634.2:n.652-32G>A
ENST00000304231.12:c.685-32G>A	ENSP00000305632.8:n.685-32G>A
ENST00000450735.6:c.652-32G>A	ENSP00000407634.2:n.652-32G>A
ENST00000558552.1:n.500G>A
ENST00000558817.1:c.409-32G>A	ENSP00000454125.1:n.409-32G>A
NM_004839.3:c.652-32G>A	NP_004830.2:n.652-32G>A
NM_199330.2:c.685-32G>A	NP_955362.1:n.685-32G>A
XM_005272448.3:c.682-32G>A	XP_005272505.1:n.682-32G>A
XM_005272449.2:c.652-32G>A	XP_005272506.1:n.652-32G>A
XM_006720775.2:c.715-32G>A	XP_006720838.1:n.715-32G>A
XM_006720776.2:c.685-32G>A	XP_006720839.1:n.685-32G>A
XM_011522231.1:c.715-32G>A	XP_011520533.1:n.715-32G>A
XM_011522232.1:c.715-32G>A	XP_011520534.1:n.715-32G>A
XM_011522233.1:c.709-32G>A	XP_011520535.1:n.709-32G>A
XM_011522234.1:c.613-32G>A	XP_011520536.1:n.613-32G>A
XM_005272448.5:c.682-32G>A	XP_005272505.1:n.682-32G>A
XM_005272449.4:c.652-32G>A	XP_005272506.1:n.652-32G>A
XM_006720775.3:c.715-32G>A	XP_006720838.1:n.715-32G>A
XM_006720776.4:c.685-32G>A	XP_006720839.1:n.685-32G>A
XM_011522231.3:c.715-32G>A	XP_011520533.1:n.715-32G>A
XM_011522232.2:c.715-32G>A	XP_011520534.1:n.715-32G>A
XM_011522233.3:c.709-32G>A	XP_011520535.1:n.709-32G>A
XM_011522234.3:c.613-32G>A	XP_011520536.1:n.613-32G>A
NM_004839.4:c.652-32G>A MANE Select	NP_004830.2:n.652-32G>A
NM_199330.3:c.685-32G>A	NP_955362.1:n.685-32G>A