Canonical Allele Identifier: CA13559053

Gene: BDNF

Linked Data

• dbSNP Id: rs10767664
• gnomAD v2: 11-27725986-T-A
• gnomAD v3: 11-27704439-T-A
• gnomAD v4: 11-27704439-T-A
• MyVariant Identifiers: chr11:g.27725986T>A (hg19) ; chr11:g.27704439T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27704439T>A , CM000673.2:g.27704439T>A	GRCh38
NC_000011.9:g.27725986T>A , CM000673.1:g.27725986T>A	GRCh37
NC_000011.8:g.27682562T>A	NCBI36
NG_011794.1:g.22620A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000314915.6:c.3+16973A>T	ENSP00000320002.6:n.3+16973A>T
ENST00000395978.7:c.-22+15990A>T	ENSP00000379302.3:n.-22+15990A>T
ENST00000395981.7:c.-22+15907A>T	ENSP00000379305.3:n.-22+15907A>T
ENST00000525950.5:c.-22+16205A>T	ENSP00000432035.1:n.-22+16205A>T
ENST00000532997.5:c.-22+15072A>T	ENSP00000435805.1:n.-22+15072A>T
NM_001143805.1:c.-22+16205A>T	NP_001137277.1:n.-22+16205A>T
NM_001143806.1:c.-22+15990A>T	NP_001137278.1:n.-22+15990A>T
NM_001143807.1:c.-22+15072A>T	NP_001137279.1:n.-22+15072A>T
NM_170731.4:c.3+16973A>T	NP_733927.1:n.3+16973A>T
NM_170732.4:c.-22+15907A>T	NP_733928.1:n.-22+15907A>T
NM_001143807.2:c.-22+15072A>T	NP_001137279.1:n.-22+15072A>T
NM_170731.5:c.3+16973A>T	NP_733927.1:n.3+16973A>T