Canonical Allele Identifier: CA219856372
Gene: BDNF HGNC NCBI

Linked Data

ClinVar Variation Id: 17698
ClinVar RCV Id: RCV000019273
dbSNP Id: rs56164415

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27700188G>A , CM000673.2:g.27700188G>A GRCh38
NC_000011.9:g.27721735G>A , CM000673.1:g.27721735G>A GRCh37
NC_000011.8:g.27678311G>A NCBI36
NG_011794.1:g.26871C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356660.9:c.-46C>T MANE Select ENSP00000349084.4:n.-46C>T
ENST00000314915.6:c.3+21224C>T ENSP00000320002.6:n.3+21224C>T
ENST00000356660.8:c.-46C>T ENSP00000349084.4:n.-46C>T
ENST00000395978.7:c.-22+20241C>T ENSP00000379302.3:n.-22+20241C>T
ENST00000395980.6:c.-22+1109C>T ENSP00000379304.2:n.-22+1109C>T
ENST00000395981.7:c.-22+20158C>T ENSP00000379305.3:n.-22+20158C>T
ENST00000395983.7:c.-22+783C>T ENSP00000379307.3:n.-22+783C>T
ENST00000418212.5:c.-153C>T ENSP00000400502.1:n.-153C>T
ENST00000420794.2:c.-422+783C>T ENSP00000389564.1:n.-422+783C>T
ENST00000438929.5:c.-59+783C>T ENSP00000414303.1:n.-59+783C>T
ENST00000525950.5:c.-22+20456C>T ENSP00000432035.1:n.-22+20456C>T
ENST00000530786.5:c.-59+783C>T ENSP00000433003.1:n.-59+783C>T
ENST00000530861.5:c.-22+488C>T ENSP00000435564.1:n.-22+488C>T
ENST00000532997.5:c.-22+19323C>T ENSP00000435805.1:n.-22+19323C>T
ENST00000533246.5:c.-28C>T ENSP00000432376.1:n.-28C>T
ENST00000584049.5:n.337+1109C>T
NM_001143805.1:c.-22+20456C>T NP_001137277.1:n.-22+20456C>T
NM_001143806.1:c.-22+20241C>T NP_001137278.1:n.-22+20241C>T
NM_001143807.1:c.-22+19323C>T NP_001137279.1:n.-22+19323C>T
NM_001143808.1:c.-22+793C>T NP_001137280.1:n.-22+793C>T
NM_001143809.1:c.66+783C>T NP_001137281.1:n.66+783C>T
NM_001143810.1:c.-59+783C>T NP_001137282.1:n.-59+783C>T
NM_001143811.1:c.-422+783C>T NP_001137283.1:n.-422+783C>T
NM_001143812.1:c.-22+488C>T NP_001137284.1:n.-22+488C>T
NM_001143813.1:c.-28C>T NP_001137285.1:n.-28C>T
NM_001143814.1:c.-153C>T NP_001137286.1:n.-153C>T
NM_001709.4:c.-46C>T NP_001700.2:n.-46C>T
NM_170731.4:c.3+21224C>T NP_733927.1:n.3+21224C>T
NM_170732.4:c.-22+20158C>T NP_733928.1:n.-22+20158C>T
NM_170733.3:c.-22+1109C>T NP_733929.1:n.-22+1109C>T
NM_001709.5:c.-46C>T MANE Select NP_001700.2:n.-46C>T
NM_001143807.2:c.-22+19323C>T NP_001137279.1:n.-22+19323C>T
NM_001143813.2:c.-28C>T NP_001137285.1:n.-28C>T
NM_001143814.2:c.-153C>T NP_001137286.1:n.-153C>T
NM_170731.5:c.3+21224C>T NP_733927.1:n.3+21224C>T
NM_001143808.2:c.-22+793C>T NP_001137280.1:n.-22+793C>T
NM_001143809.2:c.66+783C>T NP_001137281.1:n.66+783C>T
NM_001143810.2:c.-59+783C>T NP_001137282.1:n.-59+783C>T
NM_001143811.2:c.-422+783C>T NP_001137283.1:n.-422+783C>T
NM_001143812.2:c.-22+488C>T NP_001137284.1:n.-22+488C>T
NM_170733.4:c.-22+1109C>T NP_733929.1:n.-22+1109C>T