Canonical Allele Identifier: CA2580599703
Community Standard Title: NC_000011.10:g.27705368A>T
Gene: BDNF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27705368A>T , CM000673.2:g.27705368A>T GRCh38
NC_000011.9:g.27726915A>T , CM000673.1:g.27726915A>T GRCh37
NC_000011.8:g.27683491A>T NCBI36
NG_011794.1:g.21691T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001143805.1:c.-22+15276T>A NP_001137277.1:n.-22+15276T>A
NM_001143806.1:c.-22+15061T>A NP_001137278.1:n.-22+15061T>A
NM_001143807.1:c.-22+14143T>A NP_001137279.1:n.-22+14143T>A
NM_001143807.2:c.-22+14143T>A NP_001137279.1:n.-22+14143T>A
NM_170731.4:c.3+16044T>A NP_733927.1:n.3+16044T>A
NM_170731.5:c.3+16044T>A NP_733927.1:n.3+16044T>A
NM_170732.4:c.-22+14978T>A NP_733928.1:n.-22+14978T>A
ENST00000314915.6:c.3+16044T>A ENSP00000320002.6:n.3+16044T>A
ENST00000395978.7:c.-22+15061T>A ENSP00000379302.3:n.-22+15061T>A
ENST00000395981.7:c.-22+14978T>A ENSP00000379305.3:n.-22+14978T>A
ENST00000525950.5:c.-22+15276T>A ENSP00000432035.1:n.-22+15276T>A
ENST00000532997.5:c.-22+14143T>A ENSP00000435805.1:n.-22+14143T>A