Canonical Allele Identifier: CA219857028
Gene: BDNF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27706555G>A , CM000673.2:g.27706555G>A GRCh38
NC_000011.9:g.27728102G>A , CM000673.1:g.27728102G>A GRCh37
NC_000011.8:g.27684678G>A NCBI36
NG_011794.1:g.20504C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000314915.6:c.3+14857C>T ENSP00000320002.6:n.3+14857C>T
ENST00000395978.7:c.-22+13874C>T ENSP00000379302.3:n.-22+13874C>T
ENST00000395981.7:c.-22+13791C>T ENSP00000379305.3:n.-22+13791C>T
ENST00000525950.5:c.-22+14089C>T ENSP00000432035.1:n.-22+14089C>T
ENST00000532997.5:c.-22+12956C>T ENSP00000435805.1:n.-22+12956C>T
NM_001143805.1:c.-22+14089C>T NP_001137277.1:n.-22+14089C>T
NM_001143806.1:c.-22+13874C>T NP_001137278.1:n.-22+13874C>T
NM_001143807.1:c.-22+12956C>T NP_001137279.1:n.-22+12956C>T
NM_170731.4:c.3+14857C>T NP_733927.1:n.3+14857C>T
NM_170732.4:c.-22+13791C>T NP_733928.1:n.-22+13791C>T
NM_001143807.2:c.-22+12956C>T NP_001137279.1:n.-22+12956C>T
NM_170731.5:c.3+14857C>T NP_733927.1:n.3+14857C>T