Canonical Allele Identifier: CA1960124641
Community Standard Title: NC_000011.10:g.27712873T=
Gene: BDNF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27712873T= , CM000673.2:g.27712873T= GRCh38
NC_000011.9:g.27734420T= , CM000673.1:g.27734420T= GRCh37
NC_000011.8:g.27690996T= NCBI36
NG_011794.1:g.14186A=

Transcript Alleles

HGVS Amino-acid Change
NM_001143805.1:c.-22+7771A= NP_001137277.1:n.-22+7771A=
NM_001143806.1:c.-22+7556A= NP_001137278.1:n.-22+7556A=
NM_001143807.1:c.-22+6638A= NP_001137279.1:n.-22+6638A=
NM_001143807.2:c.-22+6638A= NP_001137279.1:n.-22+6638A=
NM_170731.4:c.3+8539A= NP_733927.1:n.3+8539A=
NM_170731.5:c.3+8539A= NP_733927.1:n.3+8539A=
NM_170732.4:c.-22+7473A= NP_733928.1:n.-22+7473A=
ENST00000314915.6:c.3+8539A= ENSP00000320002.6:n.3+8539A=
ENST00000395978.7:c.-22+7556A= ENSP00000379302.3:n.-22+7556A=
ENST00000395981.7:c.-22+7473A= ENSP00000379305.3:n.-22+7473A=
ENST00000525950.5:c.-22+7771A= ENSP00000432035.1:n.-22+7771A=
ENST00000532997.5:c.-22+6638A= ENSP00000435805.1:n.-22+6638A=