Canonical Allele Identifier: CA1960109505
Community Standard Title: NC_000011.10:g.27704439T=
Gene: BDNF HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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