Canonical Allele Identifier: CA219857650

Gene: BDNF

Linked Data

• dbSNP Id: rs141809511
• gnomAD v2: 11-27734351-C-T
• gnomAD v3: 11-27712804-C-T
• gnomAD v4: 11-27712804-C-T
• MyVariant Identifiers: chr11:g.27734351C>T (hg19) ; chr11:g.27712804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27712804C>T , CM000673.2:g.27712804C>T	GRCh38
NC_000011.9:g.27734351C>T , CM000673.1:g.27734351C>T	GRCh37
NC_000011.8:g.27690927C>T	NCBI36
NG_011794.1:g.14255G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314915.6:c.3+8608G>A	ENSP00000320002.6:n.3+8608G>A
ENST00000395978.7:c.-22+7625G>A	ENSP00000379302.3:n.-22+7625G>A
ENST00000395981.7:c.-22+7542G>A	ENSP00000379305.3:n.-22+7542G>A
ENST00000525950.5:c.-22+7840G>A	ENSP00000432035.1:n.-22+7840G>A
ENST00000532997.5:c.-22+6707G>A	ENSP00000435805.1:n.-22+6707G>A
NM_001143805.1:c.-22+7840G>A	NP_001137277.1:n.-22+7840G>A
NM_001143806.1:c.-22+7625G>A	NP_001137278.1:n.-22+7625G>A
NM_001143807.1:c.-22+6707G>A	NP_001137279.1:n.-22+6707G>A
NM_170731.4:c.3+8608G>A	NP_733927.1:n.3+8608G>A
NM_170732.4:c.-22+7542G>A	NP_733928.1:n.-22+7542G>A
NM_001143807.2:c.-22+6707G>A	NP_001137279.1:n.-22+6707G>A
NM_170731.5:c.3+8608G>A	NP_733927.1:n.3+8608G>A